Name: rs4148167
Published: September 21, 2022
License: Open Access

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.

rs4148167

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:119154221 (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: A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.100884 (26703/264690, TOPMED)
G=0.098889 (24824/251028, GnomAD_exome)
G=0.095573 (13395/140154, GnomAD) (+ 23 more)
G=0.104104 (12622/121244, ExAC)
G=0.11892 (9358/78692, PAGE_STUDY)
G=0.08505 (4120/48440, ALFA)
G=0.11636 (3288/28258, 14KJPN)
G=0.11523 (1931/16758, 8.3KJPN)
G=0.10470 (1360/12990, GO-ESP)
G=0.1524 (976/6404, 1000G_30x)
G=0.1538 (770/5008, 1000G)
G=0.0324 (145/4480, Estonian)
G=0.0760 (293/3854, ALSPAC)
G=0.0779 (289/3708, TWINSUK)
G=0.0414 (121/2922, KOREAN)
G=0.063 (63/998, GoNL)
G=0.075 (45/600, NorthernSweden)
G=0.076 (45/596, Vietnamese)
G=0.067 (36/534, MGP)
G=0.026 (8/304, FINRISK)
G=0.102 (22/216, Qatari)
A=0.426 (52/122, SGDP_PRJ)
G=0.06 (4/72, Ancient Sardinia)
G=0.03 (1/40, GENOME_DK)
A=0.5 (1/2, Siberian)
G=0.5 (1/2, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ABCG4 : Intron Variant
Publications: 0 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	48440	A=0.91495	G=0.08505
European	Sub	36026	A=0.92500	G=0.07500
African	Sub	4376	A=0.8505	G=0.1495
African Others	Sub	150	A=0.787	G=0.213
African American	Sub	4226	A=0.8528	G=0.1472
Asian	Sub	522	A=0.914	G=0.086
East Asian	Sub	424	A=0.927	G=0.073
Other Asian	Sub	98	A=0.86	G=0.14
Latin American 1	Sub	284	A=0.873	G=0.127
Latin American 2	Sub	1366	A=0.9327	G=0.0673
South Asian	Sub	160	A=0.750	G=0.250
Other	Sub	5706	A=0.9034	G=0.0966

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	A=0.899116	G=0.100884
gnomAD - Exomes	Global	Study-wide	251028	A=0.901111	G=0.098889
gnomAD - Exomes	European	Sub	135100	A=0.935973	G=0.064027
gnomAD - Exomes	Asian	Sub	48996	A=0.79317	G=0.20683
gnomAD - Exomes	American	Sub	34534	A=0.95170	G=0.04830
gnomAD - Exomes	African	Sub	16246	A=0.83824	G=0.16176
gnomAD - Exomes	Ashkenazi Jewish	Sub	10030	A=0.88285	G=0.11715
gnomAD - Exomes	Other	Sub	6122	A=0.9071	G=0.0929
gnomAD - Genomes	Global	Study-wide	140154	A=0.904427	G=0.095573
gnomAD - Genomes	European	Sub	75930	A=0.93590	G=0.06410
gnomAD - Genomes	African	Sub	41974	A=0.83940	G=0.16060
gnomAD - Genomes	American	Sub	13646	A=0.92555	G=0.07445
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.8905	G=0.1095
gnomAD - Genomes	East Asian	Sub	3130	A=0.9380	G=0.0620
gnomAD - Genomes	Other	Sub	2150	A=0.9009	G=0.0991
ExAC	Global	Study-wide	121244	A=0.895896	G=0.104104
ExAC	Europe	Sub	73264	A=0.93256	G=0.06744
ExAC	Asian	Sub	25126	A=0.78528	G=0.21472
ExAC	American	Sub	11546	A=0.95488	G=0.04512
ExAC	African	Sub	10402	A=0.83772	G=0.16228
ExAC	Other	Sub	906	A=0.915	G=0.085
The PAGE Study	Global	Study-wide	78692	A=0.88108	G=0.11892
The PAGE Study	AfricanAmerican	Sub	32512	A=0.84261	G=0.15739
The PAGE Study	Mexican	Sub	10806	A=0.94188	G=0.05812
The PAGE Study	Asian	Sub	8318	A=0.8717	G=0.1283
The PAGE Study	PuertoRican	Sub	7918	A=0.9198	G=0.0802
The PAGE Study	NativeHawaiian	Sub	4534	A=0.9281	G=0.0719
The PAGE Study	Cuban	Sub	4228	A=0.8985	G=0.1015
The PAGE Study	Dominican	Sub	3828	A=0.8790	G=0.1210
The PAGE Study	CentralAmerican	Sub	2450	A=0.9380	G=0.0620
The PAGE Study	SouthAmerican	Sub	1982	A=0.9258	G=0.0742
The PAGE Study	NativeAmerican	Sub	1260	A=0.9262	G=0.0738
The PAGE Study	SouthAsian	Sub	856	A=0.648	G=0.352
Allele Frequency Aggregator	Total	Global	48440	A=0.91495	G=0.08505
Allele Frequency Aggregator	European	Sub	36026	A=0.92500	G=0.07500
Allele Frequency Aggregator	Other	Sub	5706	A=0.9034	G=0.0966
Allele Frequency Aggregator	African	Sub	4376	A=0.8505	G=0.1495
Allele Frequency Aggregator	Latin American 2	Sub	1366	A=0.9327	G=0.0673
Allele Frequency Aggregator	Asian	Sub	522	A=0.914	G=0.086
Allele Frequency Aggregator	Latin American 1	Sub	284	A=0.873	G=0.127
Allele Frequency Aggregator	South Asian	Sub	160	A=0.750	G=0.250
14KJPN	JAPANESE	Study-wide	28258	A=0.88364	G=0.11636
8.3KJPN	JAPANESE	Study-wide	16758	A=0.88477	G=0.11523
GO Exome Sequencing Project	Global	Study-wide	12990	A=0.89530	G=0.10470
GO Exome Sequencing Project	European American	Sub	8590	A=0.9240	G=0.0760
GO Exome Sequencing Project	African American	Sub	4400	A=0.8393	G=0.1607
1000Genomes_30x	Global	Study-wide	6404	A=0.8476	G=0.1524
1000Genomes_30x	African	Sub	1786	A=0.8259	G=0.1741
1000Genomes_30x	Europe	Sub	1266	A=0.9171	G=0.0829
1000Genomes_30x	South Asian	Sub	1202	A=0.6697	G=0.3303
1000Genomes_30x	East Asian	Sub	1170	A=0.9103	G=0.0897
1000Genomes_30x	American	Sub	980	A=0.941	G=0.059
1000Genomes	Global	Study-wide	5008	A=0.8462	G=0.1538
1000Genomes	African	Sub	1322	A=0.8275	G=0.1725
1000Genomes	East Asian	Sub	1008	A=0.9127	G=0.0873
1000Genomes	Europe	Sub	1006	A=0.9145	G=0.0855
1000Genomes	South Asian	Sub	978	A=0.667	G=0.333
1000Genomes	American	Sub	694	A=0.939	G=0.061
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.9676	G=0.0324
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.9240	G=0.0760
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.9221	G=0.0779
KOREAN population from KRGDB	KOREAN	Study-wide	2922	A=0.9586	G=0.0414
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.937	G=0.063
Northern Sweden	ACPOP	Study-wide	600	A=0.925	G=0.075
A Vietnamese Genetic Variation Database	Global	Study-wide	596	A=0.924	G=0.076
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	A=0.933	G=0.067
FINRISK	Finnish from FINRISK project	Study-wide	304	A=0.974	G=0.026
Qatari	Global	Study-wide	216	A=0.898	G=0.102
SGDP_PRJ	Global	Study-wide	122	A=0.426	G=0.574
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	72	A=0.94	G=0.06
The Danish reference pan genome	Danish	Study-wide	40	A=0.97	G=0.03
Siberian	Global	Study-wide	2	A=0.5	G=0.5

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 11	NC_000011.10:g.119154221A>G
GRCh37.p13 chr 11	NC_000011.9:g.119024931A>G
ABCG4 RefSeqGene	NG_047178.1:g.10182A>G

Gene: ABCG4, ATP binding cassette subfamily G member 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ABCG4 transcript variant 2	NM_001142505.1:c.357-39A>G	N/A	Intron Variant
ABCG4 transcript variant 3	NM_001348191.2:c.357-39A>G	N/A	Intron Variant
ABCG4 transcript variant 4	NM_001348192.2:c.174-39A>G	N/A	Intron Variant
ABCG4 transcript variant 1	NM_022169.5:c.357-39A>G	N/A	Intron Variant
ABCG4 transcript variant X1	XM_011542952.3:c.165-39A>G	N/A	Intron Variant

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.

Not Reported in ClinVar

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	A=	G
GRCh38.p14 chr 11	NC_000011.10:g.119154221=	NC_000011.10:g.119154221A>G
GRCh37.p13 chr 11	NC_000011.9:g.119024931=	NC_000011.9:g.119024931A>G
ABCG4 RefSeqGene	NG_047178.1:g.10182=	NG_047178.1:g.10182A>G
ABCG4 transcript variant 2	NM_001142505.1:c.357-39=	NM_001142505.1:c.357-39A>G
ABCG4 transcript variant 3	NM_001348191.2:c.357-39=	NM_001348191.2:c.357-39A>G
ABCG4 transcript variant 4	NM_001348192.2:c.174-39=	NM_001348192.2:c.174-39A>G
ABCG4 transcript variant 1	NM_022169.4:c.357-39=	NM_022169.4:c.357-39A>G
ABCG4 transcript variant 1	NM_022169.5:c.357-39=	NM_022169.5:c.357-39A>G
ABCG4 transcript variant X1	XM_011542952.3:c.165-39=	XM_011542952.3:c.165-39A>G

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#.

90 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	RIKENSNPRC	ss5601902	Dec 16, 2002 (110)
2	HGSV	ss83081016	Dec 16, 2007 (130)
3	1000GENOMES	ss115256514	Jan 25, 2009 (130)
4	ILLUMINA	ss152536408	Dec 01, 2009 (131)
5	ILLUMINA	ss159102635	Dec 01, 2009 (131)
6	ILLUMINA	ss159846003	Dec 01, 2009 (131)
7	ILLUMINA	ss168870944	Jul 04, 2010 (132)
8	COMPLETE_GENOMICS	ss170996603	Jul 04, 2010 (132)
9	BUSHMAN	ss203280503	Jul 04, 2010 (132)
10	1000GENOMES	ss225491679	Jul 14, 2010 (132)
11	1000GENOMES	ss235741086	Jul 15, 2010 (132)
12	1000GENOMES	ss242335449	Jul 15, 2010 (132)
13	GMI	ss281192586	May 04, 2012 (137)
14	ILLUMINA	ss479154445	Sep 08, 2015 (146)
15	1000GENOMES	ss491030867	May 04, 2012 (137)
16	CLINSEQ_SNP	ss491655338	May 04, 2012 (137)
17	ILLUMINA	ss535359560	Sep 08, 2015 (146)
18	TISHKOFF	ss562860205	Apr 25, 2013 (138)
19	SSMP	ss658385293	Apr 25, 2013 (138)
20	NHLBI-ESP	ss713062369	Apr 25, 2013 (138)
21	ILLUMINA	ss832615431	Aug 21, 2014 (142)
22	ILLUMINA	ss833206120	Aug 21, 2014 (142)
23	EVA-GONL	ss989021020	Aug 21, 2014 (142)
24	JMKIDD_LAB	ss1067528939	Aug 21, 2014 (142)
25	JMKIDD_LAB	ss1078088824	Aug 21, 2014 (142)
26	1000GENOMES	ss1343190950	Aug 21, 2014 (142)
27	DDI	ss1426779265	Apr 01, 2015 (144)
28	EVA_GENOME_DK	ss1575986411	Apr 01, 2015 (144)
29	EVA_FINRISK	ss1584078531	Apr 01, 2015 (144)
30	EVA_DECODE	ss1598688345	Apr 01, 2015 (144)
31	EVA_UK10K_ALSPAC	ss1627584400	Apr 01, 2015 (144)
32	EVA_UK10K_TWINSUK	ss1670578433	Apr 01, 2015 (144)
33	EVA_EXAC	ss1690669540	Apr 01, 2015 (144)
34	EVA_MGP	ss1711311289	Apr 01, 2015 (144)
35	HAMMER_LAB	ss1807022252	Sep 08, 2015 (146)
36	WEILL_CORNELL_DGM	ss1932383501	Feb 12, 2016 (147)
37	ILLUMINA	ss1959391789	Feb 12, 2016 (147)
38	JJLAB	ss2026935813	Sep 14, 2016 (149)
39	USC_VALOUEV	ss2155250725	Dec 20, 2016 (150)
40	HUMAN_LONGEVITY	ss2186172472	Dec 20, 2016 (150)
41	GRF	ss2699562713	Nov 08, 2017 (151)
42	GNOMAD	ss2739446414	Nov 08, 2017 (151)
43	GNOMAD	ss2748756668	Nov 08, 2017 (151)
44	GNOMAD	ss2905091476	Nov 08, 2017 (151)
45	SWEGEN	ss3008871225	Nov 08, 2017 (151)
46	ILLUMINA	ss3021382655	Nov 08, 2017 (151)
47	BIOINF_KMB_FNS_UNIBA	ss3027269221	Nov 08, 2017 (151)
48	CSHL	ss3349821757	Nov 08, 2017 (151)
49	ILLUMINA	ss3626763706	Oct 12, 2018 (152)
50	ILLUMINA	ss3636162860	Oct 12, 2018 (152)
51	ILLUMINA	ss3637934050	Oct 12, 2018 (152)
52	OMUKHERJEE_ADBS	ss3646433718	Oct 12, 2018 (152)
53	ILLUMINA	ss3651751809	Oct 12, 2018 (152)
54	EGCUT_WGS	ss3676199336	Jul 13, 2019 (153)
55	EVA_DECODE	ss3692709928	Jul 13, 2019 (153)
56	ILLUMINA	ss3725282230	Jul 13, 2019 (153)
57	ACPOP	ss3738588691	Jul 13, 2019 (153)
58	EVA	ss3749882238	Jul 13, 2019 (153)
59	PAGE_CC	ss3771657388	Jul 13, 2019 (153)
60	KHV_HUMAN_GENOMES	ss3815210124	Jul 13, 2019 (153)
61	EVA	ss3824679210	Apr 26, 2020 (154)
62	EVA	ss3825811080	Apr 26, 2020 (154)
63	EVA	ss3832867214	Apr 26, 2020 (154)
64	EVA	ss3839996431	Apr 26, 2020 (154)
65	EVA	ss3845478414	Apr 26, 2020 (154)
66	SGDP_PRJ	ss3877253006	Apr 26, 2020 (154)
67	KRGDB	ss3925721872	Apr 26, 2020 (154)
68	FSA-LAB	ss3984015255	Apr 26, 2021 (155)
69	EVA	ss3985560915	Apr 26, 2021 (155)
70	EVA	ss3986548447	Apr 26, 2021 (155)
71	TOPMED	ss4901920956	Apr 26, 2021 (155)
72	TOMMO_GENOMICS	ss5204144677	Apr 26, 2021 (155)
73	EVA	ss5237502289	Apr 26, 2021 (155)
74	1000G_HIGH_COVERAGE	ss5289097146	Oct 16, 2022 (156)
75	EVA	ss5402607290	Oct 16, 2022 (156)
76	HUGCELL_USP	ss5484066664	Oct 16, 2022 (156)
77	1000G_HIGH_COVERAGE	ss5585679907	Oct 16, 2022 (156)
78	EVA	ss5624026401	Oct 16, 2022 (156)
79	SANFORD_IMAGENETICS	ss5624287425	Oct 16, 2022 (156)
80	SANFORD_IMAGENETICS	ss5652182783	Oct 16, 2022 (156)
81	TOMMO_GENOMICS	ss5752668395	Oct 16, 2022 (156)
82	EVA	ss5799445497	Oct 16, 2022 (156)
83	YY_MCH	ss5812825610	Oct 16, 2022 (156)
84	EVA	ss5837307704	Oct 16, 2022 (156)
85	EVA	ss5847650694	Oct 16, 2022 (156)
86	EVA	ss5848339028	Oct 16, 2022 (156)
87	EVA	ss5850174394	Oct 16, 2022 (156)
88	EVA	ss5921885776	Oct 16, 2022 (156)
89	EVA	ss5943517984	Oct 16, 2022 (156)
90	EVA	ss5979373989	Oct 16, 2022 (156)
91	1000Genomes	NC_000011.9 - 119024931	Oct 12, 2018 (152)
92	1000Genomes_30x	NC_000011.10 - 119154221	Oct 16, 2022 (156)
93	The Avon Longitudinal Study of Parents and Children	NC_000011.9 - 119024931	Oct 12, 2018 (152)
94	Genetic variation in the Estonian population	NC_000011.9 - 119024931	Oct 12, 2018 (152)
95	ExAC	NC_000011.9 - 119024931	Oct 12, 2018 (152)
96	FINRISK	NC_000011.9 - 119024931	Apr 26, 2020 (154)
97	The Danish reference pan genome	NC_000011.9 - 119024931	Apr 26, 2020 (154)
98	gnomAD - Genomes	NC_000011.10 - 119154221	Apr 26, 2021 (155)
99	gnomAD - Exomes	NC_000011.9 - 119024931	Jul 13, 2019 (153)
100	GO Exome Sequencing Project	NC_000011.9 - 119024931	Oct 12, 2018 (152)
101	Genome of the Netherlands Release 5	NC_000011.9 - 119024931	Apr 26, 2020 (154)
102	KOREAN population from KRGDB	NC_000011.9 - 119024931	Apr 26, 2020 (154)
103	Medical Genome Project healthy controls from Spanish population	NC_000011.9 - 119024931	Apr 26, 2020 (154)
104	Northern Sweden	NC_000011.9 - 119024931	Jul 13, 2019 (153)
105	The PAGE Study	NC_000011.10 - 119154221	Jul 13, 2019 (153)
106	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000011.9 - 119024931	Apr 26, 2021 (155)
107	Qatari	NC_000011.9 - 119024931	Apr 26, 2020 (154)
108	SGDP_PRJ	NC_000011.9 - 119024931	Apr 26, 2020 (154)
109	Siberian	NC_000011.9 - 119024931	Apr 26, 2020 (154)
110	8.3KJPN	NC_000011.9 - 119024931	Apr 26, 2021 (155)
111	14KJPN	NC_000011.10 - 119154221	Oct 16, 2022 (156)
112	TopMed	NC_000011.10 - 119154221	Apr 26, 2021 (155)
113	UK 10K study - Twins	NC_000011.9 - 119024931	Oct 12, 2018 (152)
114	A Vietnamese Genetic Variation Database	NC_000011.9 - 119024931	Jul 13, 2019 (153)
115	ALFA	NC_000011.10 - 119154221	Apr 26, 2021 (155)

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)
rs61622450	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss83081016, ss115256514, ss159846003, ss170996603, ss203280503, ss281192586, ss491655338, ss1598688345	NC_000011.8:118530140:A:G	NC_000011.10:119154220:A:G	(self)
55781260, 30965825, 21937584, 948261, 74992, 2758295, 8666623, 1136729, 13816352, 32899266, 427049, 11873556, 786842, 14425431, 29269986, 7767079, 62113984, 30965825, 6871368, ss225491679, ss235741086, ss242335449, ss479154445, ss491030867, ss535359560, ss562860205, ss658385293, ss713062369, ss832615431, ss833206120, ss989021020, ss1067528939, ss1078088824, ss1343190950, ss1426779265, ss1575986411, ss1584078531, ss1627584400, ss1670578433, ss1690669540, ss1711311289, ss1807022252, ss1932383501, ss1959391789, ss2026935813, ss2155250725, ss2699562713, ss2739446414, ss2748756668, ss2905091476, ss3008871225, ss3021382655, ss3349821757, ss3626763706, ss3636162860, ss3637934050, ss3646433718, ss3651751809, ss3676199336, ss3738588691, ss3749882238, ss3824679210, ss3825811080, ss3832867214, ss3839996431, ss3877253006, ss3925721872, ss3984015255, ss3985560915, ss3986548447, ss5204144677, ss5237502289, ss5402607290, ss5624026401, ss5624287425, ss5652182783, ss5799445497, ss5837307704, ss5847650694, ss5848339028, ss5943517984, ss5979373989	NC_000011.9:119024930:A:G	NC_000011.10:119154220:A:G	(self)
73205842, 393586440, 878857, 86505499, 117466612, 3940190938, ss2186172472, ss3027269221, ss3692709928, ss3725282230, ss3771657388, ss3815210124, ss3845478414, ss4901920956, ss5289097146, ss5484066664, ss5585679907, ss5752668395, ss5812825610, ss5850174394, ss5921885776	NC_000011.10:119154220:A:G	NC_000011.10:119154220:A:G	(self)
ss5601902, ss152536408, ss159102635, ss168870944	NT_033899.8:22587346:A:G	NC_000011.10:119154220:A:G	(self)

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

No publications for rs4148167

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs4148167