Name: rs10753644
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.

rs10753644

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:164722550 (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=0.319974 (84694/264690, TOPMED)
G=0.323148 (45255/140044, GnomAD)
G=0.32768 (13851/42270, ALFA) (+ 17 more)
G=0.36856 (10414/28256, 14KJPN)
G=0.36993 (6200/16760, 8.3KJPN)
G=0.3652 (2339/6404, 1000G_30x)
G=0.3710 (1858/5008, 1000G)
G=0.3094 (1386/4480, Estonian)
G=0.3435 (1324/3854, ALSPAC)
G=0.3425 (1270/3708, TWINSUK)
G=0.4096 (1200/2930, KOREAN)
G=0.4138 (758/1832, Korea1K)
G=0.3283 (371/1130, Daghestan)
G=0.350 (349/998, GoNL)
G=0.317 (190/600, NorthernSweden)
A=0.367 (116/316, SGDP_PRJ)
G=0.255 (55/216, Qatari)
G=0.40 (16/40, GENOME_DK)
A=0.42 (16/38, Siberian)
G=0.12 (2/16, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PBX1 : 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	42270	A=0.67232	G=0.32768
European	Sub	32138	A=0.67801	G=0.32199
African	Sub	4942	A=0.6305	G=0.3695
African Others	Sub	180	A=0.567	G=0.433
African American	Sub	4762	A=0.6329	G=0.3671
Asian	Sub	440	A=0.559	G=0.441
East Asian	Sub	374	A=0.556	G=0.444
Other Asian	Sub	66	A=0.58	G=0.42
Latin American 1	Sub	514	A=0.654	G=0.346
Latin American 2	Sub	836	A=0.805	G=0.195
South Asian	Sub	164	A=0.561	G=0.439
Other	Sub	3236	A=0.6693	G=0.3307

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=0.680026	G=0.319974
gnomAD - Genomes	Global	Study-wide	140044	A=0.676852	G=0.323148
gnomAD - Genomes	European	Sub	75840	A=0.68200	G=0.31800
gnomAD - Genomes	African	Sub	41968	A=0.64132	G=0.35868
gnomAD - Genomes	American	Sub	13648	A=0.77425	G=0.22575
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	A=0.7238	G=0.2762
gnomAD - Genomes	East Asian	Sub	3124	A=0.5413	G=0.4587
gnomAD - Genomes	Other	Sub	2144	A=0.6950	G=0.3050
Allele Frequency Aggregator	Total	Global	42270	A=0.67232	G=0.32768
Allele Frequency Aggregator	European	Sub	32138	A=0.67801	G=0.32199
Allele Frequency Aggregator	African	Sub	4942	A=0.6305	G=0.3695
Allele Frequency Aggregator	Other	Sub	3236	A=0.6693	G=0.3307
Allele Frequency Aggregator	Latin American 2	Sub	836	A=0.805	G=0.195
Allele Frequency Aggregator	Latin American 1	Sub	514	A=0.654	G=0.346
Allele Frequency Aggregator	Asian	Sub	440	A=0.559	G=0.441
Allele Frequency Aggregator	South Asian	Sub	164	A=0.561	G=0.439
14KJPN	JAPANESE	Study-wide	28256	A=0.63144	G=0.36856
8.3KJPN	JAPANESE	Study-wide	16760	A=0.63007	G=0.36993
1000Genomes_30x	Global	Study-wide	6404	A=0.6348	G=0.3652
1000Genomes_30x	African	Sub	1786	A=0.6389	G=0.3611
1000Genomes_30x	Europe	Sub	1266	A=0.7109	G=0.2891
1000Genomes_30x	South Asian	Sub	1202	A=0.5083	G=0.4917
1000Genomes_30x	East Asian	Sub	1170	A=0.5504	G=0.4496
1000Genomes_30x	American	Sub	980	A=0.785	G=0.215
1000Genomes	Global	Study-wide	5008	A=0.6290	G=0.3710
1000Genomes	African	Sub	1322	A=0.6415	G=0.3585
1000Genomes	East Asian	Sub	1008	A=0.5357	G=0.4643
1000Genomes	Europe	Sub	1006	A=0.7167	G=0.2833
1000Genomes	South Asian	Sub	978	A=0.501	G=0.499
1000Genomes	American	Sub	694	A=0.794	G=0.206
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.6906	G=0.3094
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.6565	G=0.3435
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.6575	G=0.3425
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.5904	G=0.4096
Korean Genome Project	KOREAN	Study-wide	1832	A=0.5862	G=0.4138
Genome-wide autozygosity in Daghestan	Global	Study-wide	1130	A=0.6717	G=0.3283
Genome-wide autozygosity in Daghestan	Daghestan	Sub	624	A=0.688	G=0.312
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.736	G=0.264
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	A=0.656	G=0.344
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.657	G=0.343
Genome-wide autozygosity in Daghestan	South Asian	Sub	96	A=0.49	G=0.51
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.72	G=0.28
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.650	G=0.350
Northern Sweden	ACPOP	Study-wide	600	A=0.683	G=0.317
SGDP_PRJ	Global	Study-wide	316	A=0.367	G=0.633
Qatari	Global	Study-wide	216	A=0.745	G=0.255
The Danish reference pan genome	Danish	Study-wide	40	A=0.60	G=0.40
Siberian	Global	Study-wide	38	A=0.42	G=0.58
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	16	A=0.88	G=0.12

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 1	NC_000001.11:g.164722550A>G
GRCh37.p13 chr 1	NC_000001.10:g.164691787A>G
PBX1 RefSeqGene	NG_028246.2:g.168191A>G

Gene: PBX1, PBX homeobox 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PBX1 transcript variant 2	NM_001204961.2:c.266-6994… NM_001204961.2:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant 3	NM_001204963.2:c.266-6994… NM_001204963.2:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant 4	NM_001353130.1:c.17-69944… NM_001353130.1:c.17-69944A>G	N/A	Intron Variant
PBX1 transcript variant 5	NM_001353131.2:c.266-6994… NM_001353131.2:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant 1	NM_002585.4:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant X3	XM_005245229.4:c.266-6994… XM_005245229.4:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant X2	XM_011509590.3:c.434-6994… XM_011509590.3:c.434-69944A>G	N/A	Intron Variant
PBX1 transcript variant X5	XM_011509592.3:c.434-6994… XM_011509592.3:c.434-69944A>G	N/A	Intron Variant
PBX1 transcript variant X4	XM_017001395.3:c.266-6994… XM_017001395.3:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant X1	XM_047421783.1:c.434-6994… XM_047421783.1:c.434-69944A>G	N/A	Intron Variant
PBX1 transcript variant X6	XM_047421784.1:c.266-6994… XM_047421784.1:c.266-69944A>G	N/A	Intron Variant
PBX1 transcript variant X7	XM_047421787.1:c.	N/A	Genic Downstream Transcript 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 1	NC_000001.11:g.164722550=	NC_000001.11:g.164722550A>G
GRCh37.p13 chr 1	NC_000001.10:g.164691787=	NC_000001.10:g.164691787A>G
PBX1 RefSeqGene	NG_028246.2:g.168191=	NG_028246.2:g.168191A>G
PBX1 transcript variant 2	NM_001204961.1:c.266-69944=	NM_001204961.1:c.266-69944A>G
PBX1 transcript variant 2	NM_001204961.2:c.266-69944=	NM_001204961.2:c.266-69944A>G
PBX1 transcript variant 3	NM_001204963.1:c.266-69944=	NM_001204963.1:c.266-69944A>G
PBX1 transcript variant 3	NM_001204963.2:c.266-69944=	NM_001204963.2:c.266-69944A>G
PBX1 transcript variant 4	NM_001353130.1:c.17-69944=	NM_001353130.1:c.17-69944A>G
PBX1 transcript variant 5	NM_001353131.2:c.266-69944=	NM_001353131.2:c.266-69944A>G
PBX1 transcript variant 1	NM_002585.3:c.266-69944=	NM_002585.3:c.266-69944A>G
PBX1 transcript variant 1	NM_002585.4:c.266-69944=	NM_002585.4:c.266-69944A>G
PBX1 transcript variant X1	XM_005245228.1:c.434-69944=	XM_005245228.1:c.434-69944A>G
PBX1 transcript variant X2	XM_005245229.1:c.266-69944=	XM_005245229.1:c.266-69944A>G
PBX1 transcript variant X3	XM_005245229.4:c.266-69944=	XM_005245229.4:c.266-69944A>G
PBX1 transcript variant X3	XM_005245230.1:c.-51+21839=	XM_005245230.1:c.-51+21839A>G
PBX1 transcript variant X2	XM_011509590.3:c.434-69944=	XM_011509590.3:c.434-69944A>G
PBX1 transcript variant X5	XM_011509592.3:c.434-69944=	XM_011509592.3:c.434-69944A>G
PBX1 transcript variant X4	XM_017001395.3:c.266-69944=	XM_017001395.3:c.266-69944A>G
PBX1 transcript variant X1	XM_047421783.1:c.434-69944=	XM_047421783.1:c.434-69944A>G
PBX1 transcript variant X6	XM_047421784.1:c.266-69944=	XM_047421784.1:c.266-69944A>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#.

82 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss16041360	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss16384551	Feb 27, 2004 (120)
3	SC_SNP	ss18136222	Feb 27, 2004 (120)
4	SC_SNP	ss18404535	Feb 27, 2004 (120)
5	SSAHASNP	ss20433192	Apr 05, 2004 (121)
6	PERLEGEN	ss23840180	Sep 20, 2004 (123)
7	ABI	ss44024987	Mar 13, 2006 (126)
8	HGSV	ss82953555	Dec 15, 2007 (130)
9	HUMANGENOME_JCVI	ss99256731	Feb 05, 2009 (130)
10	BGI	ss106606695	Feb 05, 2009 (130)
11	1000GENOMES	ss111263627	Jan 25, 2009 (130)
12	ILLUMINA-UK	ss119064623	Feb 15, 2009 (130)
13	ENSEMBL	ss131703878	Dec 01, 2009 (131)
14	ILLUMINA	ss159915448	Dec 01, 2009 (131)
15	COMPLETE_GENOMICS	ss164287393	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss165342540	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss167216529	Jul 04, 2010 (132)
18	BUSHMAN	ss199174078	Jul 04, 2010 (132)
19	1000GENOMES	ss218687996	Jul 14, 2010 (132)
20	1000GENOMES	ss230759413	Jul 14, 2010 (132)
21	1000GENOMES	ss238402072	Jul 15, 2010 (132)
22	GMI	ss276080524	May 04, 2012 (137)
23	PJP	ss290652008	May 09, 2011 (134)
24	ILLUMINA	ss479727660	Sep 08, 2015 (146)
25	TISHKOFF	ss554788909	Apr 25, 2013 (138)
26	SSMP	ss648462879	Apr 25, 2013 (138)
27	EVA-GONL	ss975757262	Aug 21, 2014 (142)
28	JMKIDD_LAB	ss1068322956	Aug 21, 2014 (142)
29	1000GENOMES	ss1293209749	Aug 21, 2014 (142)
30	HAMMER_LAB	ss1397262254	Sep 08, 2015 (146)
31	DDI	ss1426000898	Apr 01, 2015 (144)
32	EVA_GENOME_DK	ss1574441189	Apr 01, 2015 (144)
33	EVA_DECODE	ss1585141352	Apr 01, 2015 (144)
34	EVA_UK10K_ALSPAC	ss1601364030	Apr 01, 2015 (144)
35	EVA_UK10K_TWINSUK	ss1644358063	Apr 01, 2015 (144)
36	HAMMER_LAB	ss1795190359	Sep 08, 2015 (146)
37	WEILL_CORNELL_DGM	ss1918993495	Feb 12, 2016 (147)
38	GENOMED	ss1966884554	Jul 19, 2016 (147)
39	JJLAB	ss2020011674	Sep 14, 2016 (149)
40	USC_VALOUEV	ss2148038668	Dec 20, 2016 (150)
41	HUMAN_LONGEVITY	ss2167106851	Dec 20, 2016 (150)
42	SYSTEMSBIOZJU	ss2624514898	Nov 08, 2017 (151)
43	GRF	ss2698015498	Nov 08, 2017 (151)
44	GNOMAD	ss2762124180	Nov 08, 2017 (151)
45	AFFY	ss2985528478	Nov 08, 2017 (151)
46	SWEGEN	ss2987868926	Nov 08, 2017 (151)
47	ILLUMINA	ss3021146301	Nov 08, 2017 (151)
48	BIOINF_KMB_FNS_UNIBA	ss3023763294	Nov 08, 2017 (151)
49	CSHL	ss3343743871	Nov 08, 2017 (151)
50	ILLUMINA	ss3636034207	Oct 11, 2018 (152)
51	URBANLAB	ss3646807255	Oct 11, 2018 (152)
52	ILLUMINA	ss3651482783	Oct 11, 2018 (152)
53	EGCUT_WGS	ss3655809405	Jul 12, 2019 (153)
54	EVA_DECODE	ss3687922149	Jul 12, 2019 (153)
55	ILLUMINA	ss3725074410	Jul 12, 2019 (153)
56	ACPOP	ss3727548131	Jul 12, 2019 (153)
57	EVA	ss3746895036	Jul 12, 2019 (153)
58	KHV_HUMAN_GENOMES	ss3799895673	Jul 12, 2019 (153)
59	EVA	ss3826461772	Apr 25, 2020 (154)
60	EVA	ss3836626124	Apr 25, 2020 (154)
61	EVA	ss3842035836	Apr 25, 2020 (154)
62	SGDP_PRJ	ss3850152955	Apr 25, 2020 (154)
63	KRGDB	ss3895383013	Apr 25, 2020 (154)
64	KOGIC	ss3945797363	Apr 25, 2020 (154)
65	EVA	ss3984830181	Apr 25, 2021 (155)
66	TOPMED	ss4470790904	Apr 25, 2021 (155)
67	TOMMO_GENOMICS	ss5146809883	Apr 25, 2021 (155)
68	EVA	ss5237275475	Apr 25, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5244539814	Oct 12, 2022 (156)
70	HUGCELL_USP	ss5445099558	Oct 12, 2022 (156)
71	1000G_HIGH_COVERAGE	ss5517991839	Oct 12, 2022 (156)
72	SANFORD_IMAGENETICS	ss5624220254	Oct 12, 2022 (156)
73	SANFORD_IMAGENETICS	ss5626731472	Oct 12, 2022 (156)
74	TOMMO_GENOMICS	ss5674103777	Oct 12, 2022 (156)
75	YY_MCH	ss5801323038	Oct 12, 2022 (156)
76	EVA	ss5832763486	Oct 12, 2022 (156)
77	EVA	ss5847168291	Oct 12, 2022 (156)
78	EVA	ss5847560864	Oct 12, 2022 (156)
79	EVA	ss5849137712	Oct 12, 2022 (156)
80	EVA	ss5910525394	Oct 12, 2022 (156)
81	EVA	ss5938529516	Oct 12, 2022 (156)
82	EVA	ss5979293110	Oct 12, 2022 (156)
83	1000Genomes	NC_000001.10 - 164691787	Oct 11, 2018 (152)
84	1000Genomes_30x	NC_000001.11 - 164722550	Oct 12, 2022 (156)
85	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 164691787	Oct 11, 2018 (152)
86	Genome-wide autozygosity in Daghestan	NC_000001.9 - 162958411	Apr 25, 2020 (154)
87	Genetic variation in the Estonian population	NC_000001.10 - 164691787	Oct 11, 2018 (152)
88	The Danish reference pan genome	NC_000001.10 - 164691787	Apr 25, 2020 (154)
89	gnomAD - Genomes	NC_000001.11 - 164722550	Apr 25, 2021 (155)
90	Genome of the Netherlands Release 5	NC_000001.10 - 164691787	Apr 25, 2020 (154)
91	KOREAN population from KRGDB	NC_000001.10 - 164691787	Apr 25, 2020 (154)
92	Korean Genome Project	NC_000001.11 - 164722550	Apr 25, 2020 (154)
93	Northern Sweden	NC_000001.10 - 164691787	Jul 12, 2019 (153)
94	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 164691787	Apr 25, 2021 (155)
95	Qatari	NC_000001.10 - 164691787	Apr 25, 2020 (154)
96	SGDP_PRJ	NC_000001.10 - 164691787	Apr 25, 2020 (154)
97	Siberian	NC_000001.10 - 164691787	Apr 25, 2020 (154)
98	8.3KJPN	NC_000001.10 - 164691787	Apr 25, 2021 (155)
99	14KJPN	NC_000001.11 - 164722550	Oct 12, 2022 (156)
100	TopMed	NC_000001.11 - 164722550	Apr 25, 2021 (155)
101	UK 10K study - Twins	NC_000001.10 - 164691787	Oct 11, 2018 (152)
102	ALFA	NC_000001.11 - 164722550	Apr 25, 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)
rs59324964	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss82953555	NC_000001.8:161423444:A:G	NC_000001.11:164722549:A:G	(self)
23484, ss111263627, ss119064623, ss164287393, ss165342540, ss167216529, ss199174078, ss276080524, ss290652008, ss1397262254, ss1585141352	NC_000001.9:162958410:A:G	NC_000001.11:164722549:A:G	(self)
4011237, 2185577, 1547653, 1737512, 950370, 2560407, 832996, 56108, 1035425, 2169935, 555022, 4779190, 2185577, ss218687996, ss230759413, ss238402072, ss479727660, ss554788909, ss648462879, ss975757262, ss1068322956, ss1293209749, ss1426000898, ss1574441189, ss1601364030, ss1644358063, ss1795190359, ss1918993495, ss1966884554, ss2020011674, ss2148038668, ss2624514898, ss2698015498, ss2762124180, ss2985528478, ss2987868926, ss3021146301, ss3343743871, ss3636034207, ss3651482783, ss3655809405, ss3727548131, ss3746895036, ss3826461772, ss3836626124, ss3850152955, ss3895383013, ss3984830181, ss5146809883, ss5237275475, ss5624220254, ss5626731472, ss5832763486, ss5847168291, ss5847560864, ss5938529516, ss5979293110	NC_000001.10:164691786:A:G	NC_000001.11:164722549:A:G	(self)
5517774, 29104040, 2175364, 7940881, 34397239, 4973109673, ss2167106851, ss3023763294, ss3646807255, ss3687922149, ss3725074410, ss3799895673, ss3842035836, ss3945797363, ss4470790904, ss5244539814, ss5445099558, ss5517991839, ss5674103777, ss5801323038, ss5849137712, ss5910525394	NC_000001.11:164722549:A:G	NC_000001.11:164722549:A:G	(self)
ss23840180, ss44024987, ss99256731, ss106606695, ss131703878, ss159915448	NT_004487.19:16180428:A:G	NC_000001.11:164722549:A:G	(self)
ss16041360, ss16384551, ss18136222, ss18404535, ss20433192	NT_004668.16:3197258:A:G	NC_000001.11:164722549: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 rs10753644

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10753644