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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs11168070

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:148826364 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
G>A / G>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.304254 (80533/264690, TOPMED)
G=0.322725 (45206/140076, GnomAD)
G=0.06158 (1740/28258, 14KJPN) (+ 17 more)
G=0.37660 (7114/18890, ALFA)
G=0.06056 (1015/16760, 8.3KJPN)
G=0.34726 (3733/10750, PharmGKB)
G=0.2063 (1321/6404, 1000G_30x)
G=0.2041 (1022/5008, 1000G)
G=0.4248 (1903/4480, Estonian)
G=0.4354 (1678/3854, ALSPAC)
G=0.4442 (1647/3708, TWINSUK)
G=0.1052 (308/2928, KOREAN)
G=0.1060 (194/1830, Korea1K)
G=0.407 (244/600, NorthernSweden)
G=0.138 (72/520, SGDP_PRJ)
G=0.222 (48/216, Qatari)
G=0.065 (14/214, Vietnamese)
G=0.131 (27/206, HapMap)
G=0.29 (14/48, Siberian)
C=0.30 (12/40, GENOME_DK)
Clinical Significance
Reported in ClinVar
Gene : Consequence
ADRB2 : 2KB Upstream Variant
Publications
8 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 18890 G=0.37660 C=0.62340
European Sub 14286 G=0.43126 C=0.56874
African Sub 2946 G=0.1833 C=0.8167
African Others Sub 114 G=0.158 C=0.842
African American Sub 2832 G=0.1843 C=0.8157
Asian Sub 112 G=0.152 C=0.848
East Asian Sub 86 G=0.13 C=0.87
Other Asian Sub 26 G=0.23 C=0.77
Latin American 1 Sub 146 G=0.274 C=0.726
Latin American 2 Sub 610 G=0.205 C=0.795
South Asian Sub 98 G=0.17 C=0.83
Other Sub 692 G=0.309 C=0.691


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
TopMed Global Study-wide 264690 G=0.304254 C=0.695746
gnomAD - Genomes Global Study-wide 140076 G=0.322725 C=0.677275
gnomAD - Genomes European Sub 75856 G=0.42295 C=0.57705
gnomAD - Genomes African Sub 41974 G=0.18095 C=0.81905
gnomAD - Genomes American Sub 13650 G=0.24410 C=0.75590
gnomAD - Genomes Ashkenazi Jewish Sub 3318 G=0.3716 C=0.6284
gnomAD - Genomes East Asian Sub 3132 G=0.0983 C=0.9017
gnomAD - Genomes Other Sub 2146 G=0.3052 C=0.6948
14KJPN JAPANESE Study-wide 28258 G=0.06158 C=0.93842
Allele Frequency Aggregator Total Global 18890 G=0.37660 C=0.62340
Allele Frequency Aggregator European Sub 14286 G=0.43126 C=0.56874
Allele Frequency Aggregator African Sub 2946 G=0.1833 C=0.8167
Allele Frequency Aggregator Other Sub 692 G=0.309 C=0.691
Allele Frequency Aggregator Latin American 2 Sub 610 G=0.205 C=0.795
Allele Frequency Aggregator Latin American 1 Sub 146 G=0.274 C=0.726
Allele Frequency Aggregator Asian Sub 112 G=0.152 C=0.848
Allele Frequency Aggregator South Asian Sub 98 G=0.17 C=0.83
8.3KJPN JAPANESE Study-wide 16760 G=0.06056 C=0.93944
PharmGKB Aggregated Global Study-wide 10750 G=0.34726 C=0.65274
PharmGKB Aggregated PA142013869 Sub 4310 G=0.3677 C=0.6323
PharmGKB Aggregated PA143260469 Sub 2774 G=0.3180 C=0.6820
PharmGKB Aggregated PA128523252 Sub 1888 G=0.3400 C=0.6600
PharmGKB Aggregated PA129185709 Sub 650 G=0.329 C=0.671
PharmGKB Aggregated PA130625709 Sub 592 G=0.355 C=0.645
PharmGKB Aggregated PA129947797 Sub 446 G=0.386 C=0.614
PharmGKB Aggregated PA142648497 Sub 90 G=0.31 C=0.69
1000Genomes_30x Global Study-wide 6404 G=0.2063 C=0.7937
1000Genomes_30x African Sub 1786 G=0.1372 C=0.8628
1000Genomes_30x Europe Sub 1266 G=0.4186 C=0.5814
1000Genomes_30x South Asian Sub 1202 G=0.1938 C=0.8062
1000Genomes_30x East Asian Sub 1170 G=0.0709 C=0.9291
1000Genomes_30x American Sub 980 G=0.235 C=0.765
1000Genomes Global Study-wide 5008 G=0.2041 C=0.7959
1000Genomes African Sub 1322 G=0.1377 C=0.8623
1000Genomes East Asian Sub 1008 G=0.0724 C=0.9276
1000Genomes Europe Sub 1006 G=0.4085 C=0.5915
1000Genomes South Asian Sub 978 G=0.194 C=0.806
1000Genomes American Sub 694 G=0.239 C=0.761
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.4248 C=0.5752
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.4354 C=0.5646
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.4442 C=0.5558
KOREAN population from KRGDB KOREAN Study-wide 2928 G=0.1052 A=0.0000, C=0.8948, T=0.0000
Korean Genome Project KOREAN Study-wide 1830 G=0.1060 C=0.8940
Northern Sweden ACPOP Study-wide 600 G=0.407 C=0.593
SGDP_PRJ Global Study-wide 520 G=0.138 C=0.862
Qatari Global Study-wide 216 G=0.222 C=0.778
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.065 C=0.935
HapMap Global Study-wide 206 G=0.131 C=0.869
HapMap African Sub 118 G=0.169 C=0.831
HapMap Asian Sub 88 G=0.08 C=0.92
Siberian Global Study-wide 48 G=0.29 C=0.71
The Danish reference pan genome Danish Study-wide 40 G=0.70 C=0.30
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 5 NC_000005.10:g.148826364G>A
GRCh38.p14 chr 5 NC_000005.10:g.148826364G>C
GRCh38.p14 chr 5 NC_000005.10:g.148826364G>T
GRCh37.p13 chr 5 NC_000005.9:g.148205927G>A
GRCh37.p13 chr 5 NC_000005.9:g.148205927G>C
GRCh37.p13 chr 5 NC_000005.9:g.148205927G>T
ADRB2 RefSeqGene NG_016421.2:g.4772G>A
ADRB2 RefSeqGene NG_016421.2:g.4772G>C
ADRB2 RefSeqGene NG_016421.2:g.4772G>T
Gene: ADRB2, adrenoceptor beta 2 (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
ADRB2 transcript NM_000024.6:c. N/A Upstream Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: C (allele ID: 1222924 )
ClinVar Accession Disease Names Clinical Significance
RCV001621859.3 not provided Benign
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement G= A C T
GRCh38.p14 chr 5 NC_000005.10:g.148826364= NC_000005.10:g.148826364G>A NC_000005.10:g.148826364G>C NC_000005.10:g.148826364G>T
GRCh37.p13 chr 5 NC_000005.9:g.148205927= NC_000005.9:g.148205927G>A NC_000005.9:g.148205927G>C NC_000005.9:g.148205927G>T
ADRB2 RefSeqGene NG_016421.2:g.4772= NG_016421.2:g.4772G>A NG_016421.2:g.4772G>C NG_016421.2:g.4772G>T
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

116 SubSNP, 20 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss17841652 Feb 27, 2004 (120)
2 CSHL-HAPMAP ss20240208 Feb 27, 2004 (120)
3 SSAHASNP ss22327267 Apr 05, 2004 (121)
4 IMCJ-GDT ss22886611 Apr 05, 2004 (121)
5 ABI ss44588841 Mar 11, 2006 (126)
6 PGA-UW-FHCRC ss46533158 Mar 11, 2006 (126)
7 UCSF_HG ss49783222 Mar 11, 2006 (126)
8 STEJUSTINE-REGGEN ss51853097 Mar 16, 2006 (126)
9 ILLUMINA ss65725193 Oct 15, 2006 (127)
10 TAPPERS ss69358153 May 17, 2007 (127)
11 PHARMGKB_PCE ss69365444 May 17, 2007 (127)
12 PHARMGKB_PAAR-SJCRH ss69367523 May 17, 2007 (127)
13 PHARMGKB_PHAT ss69368300 May 17, 2007 (127)
14 PHARMGKB_APP ss69369803 May 17, 2007 (127)
15 PHARMGKB_APP ss69370070 May 17, 2007 (127)
16 PHARMGKB_APP ss69370309 May 17, 2007 (127)
17 AFFY ss74807389 Aug 16, 2007 (128)
18 HGSV ss82718455 Dec 15, 2007 (130)
19 HGSV ss85135806 Dec 15, 2007 (130)
20 BCMHGSC_JDW ss93286303 Mar 24, 2008 (129)
21 HUMANGENOME_JCVI ss98775113 Feb 05, 2009 (130)
22 BGI ss105958859 Feb 05, 2009 (130)
23 1000GENOMES ss109502581 Jan 24, 2009 (130)
24 1000GENOMES ss113428955 Jan 25, 2009 (130)
25 ILLUMINA-UK ss116853623 Feb 14, 2009 (130)
26 ENSEMBL ss142625138 Dec 01, 2009 (131)
27 ENSEMBL ss143519806 Dec 01, 2009 (131)
28 GMI ss156154917 Dec 01, 2009 (131)
29 ILLUMINA ss159965844 Dec 01, 2009 (131)
30 COMPLETE_GENOMICS ss162755474 Jul 04, 2010 (132)
31 COMPLETE_GENOMICS ss165962389 Jul 04, 2010 (132)
32 ILLUMINA ss171118253 Jul 04, 2010 (132)
33 PHARMGKB_PHAT ss181129023 Jul 04, 2010 (132)
34 BUSHMAN ss201006913 Jul 04, 2010 (132)
35 BCM-HGSC-SUB ss207078710 Jul 04, 2010 (132)
36 1000GENOMES ss222028636 Jul 14, 2010 (132)
37 1000GENOMES ss233192407 Jul 14, 2010 (132)
38 1000GENOMES ss240305949 Jul 15, 2010 (132)
39 GMI ss278525017 May 04, 2012 (137)
40 PJP ss293490458 May 09, 2011 (134)
41 ILLUMINA ss479485884 May 04, 2012 (137)
42 ILLUMINA ss479489870 May 04, 2012 (137)
43 ILLUMINA ss479929148 Sep 08, 2015 (146)
44 ILLUMINA ss484542468 May 04, 2012 (137)
45 ILLUMINA ss536682354 Sep 08, 2015 (146)
46 TISHKOFF ss558785518 Apr 25, 2013 (138)
47 SSMP ss652689231 Apr 25, 2013 (138)
48 ILLUMINA ss778718351 Sep 08, 2015 (146)
49 ILLUMINA ss782717870 Sep 08, 2015 (146)
50 ILLUMINA ss783685497 Sep 08, 2015 (146)
51 ILLUMINA ss831969365 Sep 08, 2015 (146)
52 ILLUMINA ss834177710 Sep 08, 2015 (146)
53 EVA-GONL ss982244492 Aug 21, 2014 (142)
54 JMKIDD_LAB ss1073130449 Aug 21, 2014 (142)
55 1000GENOMES ss1317693427 Aug 21, 2014 (142)
56 DDI ss1430535514 Apr 01, 2015 (144)
57 EVA_GENOME_DK ss1581396231 Apr 01, 2015 (144)
58 EVA_DECODE ss1591776840 Apr 01, 2015 (144)
59 EVA_UK10K_ALSPAC ss1614268101 Apr 01, 2015 (144)
60 EVA_UK10K_TWINSUK ss1657262134 Apr 01, 2015 (144)
61 ILLUMINA ss1752555221 Sep 08, 2015 (146)
62 HAMMER_LAB ss1804132070 Sep 08, 2015 (146)
63 WEILL_CORNELL_DGM ss1925498514 Feb 12, 2016 (147)
64 GENOMED ss1970234525 Jul 19, 2016 (147)
65 JJLAB ss2023356555 Sep 14, 2016 (149)
66 USC_VALOUEV ss2151515046 Dec 20, 2016 (150)
67 HUMAN_LONGEVITY ss2279156535 Dec 20, 2016 (150)
68 SYSTEMSBIOZJU ss2626166623 Nov 08, 2017 (151)
69 ILLUMINA ss2634354522 Nov 08, 2017 (151)
70 GRF ss2707084326 Nov 08, 2017 (151)
71 GNOMAD ss2832147545 Nov 08, 2017 (151)
72 SWEGEN ss2997982670 Nov 08, 2017 (151)
73 ILLUMINA ss3022540960 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3025460088 Nov 08, 2017 (151)
75 CSHL ss3346678466 Nov 08, 2017 (151)
76 ILLUMINA ss3629367625 Oct 12, 2018 (152)
77 ILLUMINA ss3632277637 Oct 12, 2018 (152)
78 ILLUMINA ss3633393763 Oct 12, 2018 (152)
79 ILLUMINA ss3634115125 Oct 12, 2018 (152)
80 ILLUMINA ss3635027927 Oct 12, 2018 (152)
81 ILLUMINA ss3635796772 Oct 12, 2018 (152)
82 ILLUMINA ss3636741118 Oct 12, 2018 (152)
83 ILLUMINA ss3637549428 Oct 12, 2018 (152)
84 ILLUMINA ss3638587571 Oct 12, 2018 (152)
85 ILLUMINA ss3640735221 Oct 12, 2018 (152)
86 URBANLAB ss3648194718 Oct 12, 2018 (152)
87 ILLUMINA ss3653043939 Oct 12, 2018 (152)
88 EGCUT_WGS ss3665902707 Jul 13, 2019 (153)
89 EVA_DECODE ss3715930571 Jul 13, 2019 (153)
90 ILLUMINA ss3726280658 Jul 13, 2019 (153)
91 ACPOP ss3732916307 Jul 13, 2019 (153)
92 ILLUMINA ss3745328101 Jul 13, 2019 (153)
93 EVA ss3764207353 Jul 13, 2019 (153)
94 ILLUMINA ss3772822056 Jul 13, 2019 (153)
95 KHV_HUMAN_GENOMES ss3807376586 Jul 13, 2019 (153)
96 EVA ss3829561444 Apr 26, 2020 (154)
97 EVA ss3838254705 Apr 26, 2020 (154)
98 EVA ss3843697748 Apr 26, 2020 (154)
99 SGDP_PRJ ss3863219816 Apr 26, 2020 (154)
100 KRGDB ss3909894962 Apr 26, 2020 (154)
101 KOGIC ss3957872230 Apr 26, 2020 (154)
102 EVA ss4017237512 Apr 26, 2021 (155)
103 TOPMED ss4682905053 Apr 26, 2021 (155)
104 TOMMO_GENOMICS ss5174682985 Apr 26, 2021 (155)
105 1000G_HIGH_COVERAGE ss5266260605 Oct 13, 2022 (156)
106 EVA ss5315094237 Oct 13, 2022 (156)
107 EVA ss5361730364 Oct 13, 2022 (156)
108 HUGCELL_USP ss5464182316 Oct 13, 2022 (156)
109 1000G_HIGH_COVERAGE ss5551124884 Oct 13, 2022 (156)
110 SANFORD_IMAGENETICS ss5639116910 Oct 13, 2022 (156)
111 TOMMO_GENOMICS ss5711918926 Oct 13, 2022 (156)
112 YY_MCH ss5806865889 Oct 13, 2022 (156)
113 EVA ss5835802308 Oct 13, 2022 (156)
114 EVA ss5855064158 Oct 13, 2022 (156)
115 EVA ss5896806200 Oct 13, 2022 (156)
116 EVA ss5967595832 Oct 13, 2022 (156)
117 1000Genomes NC_000005.9 - 148205927 Oct 12, 2018 (152)
118 1000Genomes_30x NC_000005.10 - 148826364 Oct 13, 2022 (156)
119 The Avon Longitudinal Study of Parents and Children NC_000005.9 - 148205927 Oct 12, 2018 (152)
120 Genetic variation in the Estonian population NC_000005.9 - 148205927 Oct 12, 2018 (152)
121 The Danish reference pan genome NC_000005.9 - 148205927 Apr 26, 2020 (154)
122 gnomAD - Genomes NC_000005.10 - 148826364 Apr 26, 2021 (155)
123 HapMap NC_000005.10 - 148826364 Apr 26, 2020 (154)
124 KOREAN population from KRGDB NC_000005.9 - 148205927 Apr 26, 2020 (154)
125 Korean Genome Project NC_000005.10 - 148826364 Apr 26, 2020 (154)
126 Northern Sweden NC_000005.9 - 148205927 Jul 13, 2019 (153)
127 PharmGKB Aggregated NC_000005.10 - 148826364 Apr 26, 2020 (154)
128 Qatari NC_000005.9 - 148205927 Apr 26, 2020 (154)
129 SGDP_PRJ NC_000005.9 - 148205927 Apr 26, 2020 (154)
130 Siberian NC_000005.9 - 148205927 Apr 26, 2020 (154)
131 8.3KJPN NC_000005.9 - 148205927 Apr 26, 2021 (155)
132 14KJPN NC_000005.10 - 148826364 Oct 13, 2022 (156)
133 TopMed NC_000005.10 - 148826364 Apr 26, 2021 (155)
134 UK 10K study - Twins NC_000005.9 - 148205927 Oct 12, 2018 (152)
135 A Vietnamese Genetic Variation Database NC_000005.9 - 148205927 Jul 13, 2019 (153)
136 ALFA NC_000005.10 - 148826364 Apr 26, 2021 (155)
137 ClinVar RCV001621859.3 Oct 13, 2022 (156)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs17334166 Mar 11, 2006 (126)
rs17334221 Mar 11, 2006 (126)
rs36217682 Oct 25, 2006 (127)
rs52827606 Sep 21, 2007 (128)
rs59587862 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
17072356, ss3909894962 NC_000005.9:148205926:G:A NC_000005.10:148826363:G:A (self)
ss82718455, ss85135806, ss93286303, ss109502581, ss113428955, ss116853623, ss159965844, ss162755474, ss165962389, ss201006913, ss207078710, ss278525017, ss293490458, ss479485884, ss1591776840 NC_000005.8:148186119:G:C NC_000005.10:148826363:G:C (self)
29388902, 16351749, 11640955, 7561170, 17072356, 6201172, 7540444, 15236796, 4031400, 32652292, 16351749, 3624061, ss222028636, ss233192407, ss240305949, ss479489870, ss479929148, ss484542468, ss536682354, ss558785518, ss652689231, ss778718351, ss782717870, ss783685497, ss831969365, ss834177710, ss982244492, ss1073130449, ss1317693427, ss1430535514, ss1581396231, ss1614268101, ss1657262134, ss1752555221, ss1804132070, ss1925498514, ss1970234525, ss2023356555, ss2151515046, ss2626166623, ss2634354522, ss2707084326, ss2832147545, ss2997982670, ss3022540960, ss3346678466, ss3629367625, ss3632277637, ss3633393763, ss3634115125, ss3635027927, ss3635796772, ss3636741118, ss3637549428, ss3638587571, ss3640735221, ss3653043939, ss3665902707, ss3732916307, ss3745328101, ss3764207353, ss3772822056, ss3829561444, ss3838254705, ss3863219816, ss3909894962, ss4017237512, ss5174682985, ss5315094237, ss5361730364, ss5639116910, ss5835802308, ss5967595832 NC_000005.9:148205926:G:C NC_000005.10:148826363:G:C (self)
RCV001621859.3, 38650819, 207885584, 2992214, 14250231, 10492, 45756030, 520282610, 1903545329, ss2279156535, ss3025460088, ss3648194718, ss3715930571, ss3726280658, ss3807376586, ss3843697748, ss3957872230, ss4682905053, ss5266260605, ss5464182316, ss5551124884, ss5711918926, ss5806865889, ss5855064158, ss5896806200 NC_000005.10:148826363:G:C NC_000005.10:148826363:G:C (self)
ss17841652, ss20240208, ss22327267 NT_029289.10:9368862:G:C NC_000005.10:148826363:G:C (self)
ss22886611, ss44588841, ss46533158, ss49783222, ss51853097, ss65725193, ss69358153, ss69365444, ss69367523, ss69368300, ss69369803, ss69370070, ss69370309, ss74807389, ss98775113, ss105958859, ss142625138, ss143519806, ss156154917, ss171118253, ss181129023 NT_029289.11:9368853:G:C NC_000005.10:148826363:G:C (self)
17072356, ss3909894962 NC_000005.9:148205926:G:T NC_000005.10:148826363:G:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

8 citations for rs11168070
PMID Title Author Year Journal
18182569 Pharmacogenetics of minimal residual disease response in children with B-precursor acute lymphoblastic leukemia: a report from the Children's Oncology Group. Davies SM et al. 2008 Blood
19284637 Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence. Chu X et al. 2009 BMC medical genetics
20537997 Genetic covariance between gamma-glutamyl transpeptidase and fatty liver risk factors: role of beta2-adrenergic receptor genetic variation in twins. Loomba R et al. 2010 Gastroenterology
21387019 Differences in candidate gene association between European ancestry and African American asthmatic children. Baye TM et al. 2011 PloS one
26339405 Relationship between the single nucleotide polymorphisms of β₂-adrenergic receptor 5'-regulatory region and essential hypertension in Chinese Kazakh ethnic minority group. Cai W et al. 2015 International journal of clinical and experimental pathology
30837870 Beta2-Adrenergic Receptor Polymorphisms and Haplotypes Associate With Chronic Pain in Sickle Cell Disease. Jhun EH et al. 2019 Frontiers in pharmacology
31855300 Epistasis between phenylethanolamine N-methyltransferase and β2-adrenergic receptor influences extracellular epinephrine level and associates with the susceptibility to allergic asthma. Sio YY et al. 2020 Clinical and experimental allergy
34753545 Association between ADRB2 regulatory region polymorphisms and susceptibility to childhood asthma. Cai MX et al. 2021 Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post761+d5e8e07