Name: rs10127740
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.

rs10127740

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:54236552 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.274752 (72724/264690, TOPMED)
T=0.279436 (39154/140118, GnomAD)
T=0.11724 (3313/28258, 14KJPN) (+ 17 more)
T=0.30083 (6484/21554, ALFA)
T=0.11581 (1941/16760, 8.3KJPN)
T=0.2416 (1547/6404, 1000G_30x)
T=0.2428 (1216/5008, 1000G)
T=0.3089 (1384/4480, Estonian)
T=0.3313 (1277/3854, ALSPAC)
T=0.3010 (1116/3708, TWINSUK)
T=0.1485 (435/2930, KOREAN)
T=0.1386 (254/1832, Korea1K)
T=0.305 (304/998, GoNL)
T=0.302 (181/600, NorthernSweden)
T=0.000 (0/318, HapMap)
G=0.430 (99/230, SGDP_PRJ)
T=0.264 (57/216, Qatari)
T=0.215 (46/214, Vietnamese)
T=0.25 (10/40, GENOME_DK)
G=0.45 (9/20, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SSBP3-AS1 : Non Coding Transcript Variant
SSBP3 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	21554	G=0.69917	T=0.30083	0.490303	0.091955	0.417741	0
European	Sub	14314	G=0.69142	T=0.30858	0.481626	0.098784	0.419589	1
African	Sub	3240	G=0.7284	T=0.2716	0.529012	0.072222	0.398765	0
African Others	Sub	114	G=0.684	T=0.316	0.491228	0.122807	0.385965	0
African American	Sub	3126	G=0.7300	T=0.2700	0.53039	0.070377	0.399232	0
Asian	Sub	134	G=0.784	T=0.216	0.597015	0.029851	0.373134	0
East Asian	Sub	104	G=0.788	T=0.212	0.615385	0.038462	0.346154	0
Other Asian	Sub	30	G=0.77	T=0.23	0.533333	0.0	0.466667	1
Latin American 1	Sub	160	G=0.731	T=0.269	0.55	0.0875	0.3625	0
Latin American 2	Sub	642	G=0.734	T=0.266	0.529595	0.062305	0.4081	0
South Asian	Sub	114	G=0.719	T=0.281	0.508772	0.070175	0.421053	0
Other	Sub	2950	G=0.6908	T=0.3092	0.472542	0.090847	0.43661	0

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	G=0.725248	T=0.274752
gnomAD - Genomes	Global	Study-wide	140118	G=0.720564	T=0.279436
gnomAD - Genomes	European	Sub	75898	G=0.70035	T=0.29965
gnomAD - Genomes	African	Sub	41974	G=0.73965	T=0.26035
gnomAD - Genomes	American	Sub	13644	G=0.74077	T=0.25923
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.7464	T=0.2536
gnomAD - Genomes	East Asian	Sub	3132	G=0.8276	T=0.1724
gnomAD - Genomes	Other	Sub	2146	G=0.7377	T=0.2623
14KJPN	JAPANESE	Study-wide	28258	G=0.88276	T=0.11724
Allele Frequency Aggregator	Total	Global	21554	G=0.69917	T=0.30083
Allele Frequency Aggregator	European	Sub	14314	G=0.69142	T=0.30858
Allele Frequency Aggregator	African	Sub	3240	G=0.7284	T=0.2716
Allele Frequency Aggregator	Other	Sub	2950	G=0.6908	T=0.3092
Allele Frequency Aggregator	Latin American 2	Sub	642	G=0.734	T=0.266
Allele Frequency Aggregator	Latin American 1	Sub	160	G=0.731	T=0.269
Allele Frequency Aggregator	Asian	Sub	134	G=0.784	T=0.216
Allele Frequency Aggregator	South Asian	Sub	114	G=0.719	T=0.281
8.3KJPN	JAPANESE	Study-wide	16760	G=0.88419	T=0.11581
1000Genomes_30x	Global	Study-wide	6404	G=0.7584	T=0.2416
1000Genomes_30x	African	Sub	1786	G=0.7710	T=0.2290
1000Genomes_30x	Europe	Sub	1266	G=0.7030	T=0.2970
1000Genomes_30x	South Asian	Sub	1202	G=0.7546	T=0.2454
1000Genomes_30x	East Asian	Sub	1170	G=0.8299	T=0.1701
1000Genomes_30x	American	Sub	980	G=0.727	T=0.273
1000Genomes	Global	Study-wide	5008	G=0.7572	T=0.2428
1000Genomes	African	Sub	1322	G=0.7723	T=0.2277
1000Genomes	East Asian	Sub	1008	G=0.8323	T=0.1677
1000Genomes	Europe	Sub	1006	G=0.6998	T=0.3002
1000Genomes	South Asian	Sub	978	G=0.751	T=0.249
1000Genomes	American	Sub	694	G=0.712	T=0.288
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.6911	T=0.3089
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.6687	T=0.3313
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.6990	T=0.3010
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.8515	T=0.1485
Korean Genome Project	KOREAN	Study-wide	1832	G=0.8614	T=0.1386
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.695	T=0.305
Northern Sweden	ACPOP	Study-wide	600	G=0.698	T=0.302
HapMap	Global	Study-wide	318	G=1.000	T=0.000
HapMap	African	Sub	116	G=1.000	T=0.000
HapMap	American	Sub	114	G=1.000	T=0.000
HapMap	Asian	Sub	88	G=1.00	T=0.00
SGDP_PRJ	Global	Study-wide	230	G=0.430	T=0.570
Qatari	Global	Study-wide	216	G=0.736	T=0.264
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.785	T=0.215
The Danish reference pan genome	Danish	Study-wide	40	G=0.75	T=0.25
Siberian	Global	Study-wide	20	G=0.45	T=0.55

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.54236552G>T
GRCh37.p13 chr 1	NC_000001.10:g.54702225G>T

Gene: SSBP3, single stranded DNA binding protein 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SSBP3 transcript variant 3	NM_001009955.4:c.846+2577… NM_001009955.4:c.846+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 4	NM_001394360.1:c.870+2577… NM_001394360.1:c.870+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 5	NM_001394361.1:c.807+2577… NM_001394361.1:c.807+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 6	NM_001394362.1:c.786+2577… NM_001394362.1:c.786+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 7	NM_001394363.1:c.696+2577… NM_001394363.1:c.696+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 8	NM_001394364.1:c.597+2577… NM_001394364.1:c.597+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 9	NM_001394365.1:c.516+2577… NM_001394365.1:c.516+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 10	NM_001394366.1:c.516+2577… NM_001394366.1:c.516+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 11	NM_001394367.1:c.480+2577… NM_001394367.1:c.480+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 2	NM_018070.5:c.867+2577C>A	N/A	Intron Variant
SSBP3 transcript variant 1	NM_145716.4:c.927+2577C>A	N/A	Intron Variant
SSBP3 transcript variant X4	XM_017000897.3:c.597+2577… XM_017000897.3:c.597+2577C>A	N/A	Intron Variant
SSBP3 transcript variant X6	XM_017000898.3:c.597+2577… XM_017000898.3:c.597+2577C>A	N/A	Intron Variant
SSBP3 transcript variant X1	XM_047416692.1:c.597+2577… XM_047416692.1:c.597+2577C>A	N/A	Intron Variant
SSBP3 transcript variant X2	XM_047416693.1:c.516+2577… XM_047416693.1:c.516+2577C>A	N/A	Intron Variant
SSBP3 transcript variant X3	XM_047416695.1:c.456+2577… XM_047416695.1:c.456+2577C>A	N/A	Intron Variant
SSBP3 transcript variant X5	XM_047416697.1:c.516+2577… XM_047416697.1:c.516+2577C>A	N/A	Intron Variant

Gene: SSBP3-AS1, SSBP3 antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SSBP3-AS1 transcript	NR_103541.1:n.110G>T	N/A	Non Coding 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	G=	T
GRCh38.p14 chr 1	NC_000001.11:g.54236552=	NC_000001.11:g.54236552G>T
GRCh37.p13 chr 1	NC_000001.10:g.54702225=	NC_000001.10:g.54702225G>T
SSBP3-AS1 transcript	NR_103541.1:n.110=	NR_103541.1:n.110G>T
SSBP3 transcript variant 3	NM_001009955.3:c.846+2577=	NM_001009955.3:c.846+2577C>A
SSBP3 transcript variant 3	NM_001009955.4:c.846+2577=	NM_001009955.4:c.846+2577C>A
SSBP3 transcript variant 4	NM_001394360.1:c.870+2577=	NM_001394360.1:c.870+2577C>A
SSBP3 transcript variant 5	NM_001394361.1:c.807+2577=	NM_001394361.1:c.807+2577C>A
SSBP3 transcript variant 6	NM_001394362.1:c.786+2577=	NM_001394362.1:c.786+2577C>A
SSBP3 transcript variant 7	NM_001394363.1:c.696+2577=	NM_001394363.1:c.696+2577C>A
SSBP3 transcript variant 8	NM_001394364.1:c.597+2577=	NM_001394364.1:c.597+2577C>A
SSBP3 transcript variant 9	NM_001394365.1:c.516+2577=	NM_001394365.1:c.516+2577C>A
SSBP3 transcript variant 10	NM_001394366.1:c.516+2577=	NM_001394366.1:c.516+2577C>A
SSBP3 transcript variant 11	NM_001394367.1:c.480+2577=	NM_001394367.1:c.480+2577C>A
SSBP3 transcript variant 2	NM_018070.4:c.867+2577=	NM_018070.4:c.867+2577C>A
SSBP3 transcript variant 2	NM_018070.5:c.867+2577=	NM_018070.5:c.867+2577C>A
SSBP3 transcript variant 1	NM_145716.3:c.927+2577=	NM_145716.3:c.927+2577C>A
SSBP3 transcript variant 1	NM_145716.4:c.927+2577=	NM_145716.4:c.927+2577C>A
SSBP3 transcript variant X1	XM_005270712.1:c.951+2577=	XM_005270712.1:c.951+2577C>A
SSBP3 transcript variant X2	XM_005270713.1:c.870+2577=	XM_005270713.1:c.870+2577C>A
SSBP3 transcript variant X3	XM_005270714.1:c.780+2577=	XM_005270714.1:c.780+2577C>A
SSBP3 transcript variant X4	XM_005270715.1:c.756+2577=	XM_005270715.1:c.756+2577C>A
SSBP3 transcript variant X4	XM_017000897.3:c.597+2577=	XM_017000897.3:c.597+2577C>A
SSBP3 transcript variant X6	XM_017000898.3:c.597+2577=	XM_017000898.3:c.597+2577C>A
SSBP3 transcript variant X1	XM_047416692.1:c.597+2577=	XM_047416692.1:c.597+2577C>A
SSBP3 transcript variant X2	XM_047416693.1:c.516+2577=	XM_047416693.1:c.516+2577C>A
SSBP3 transcript variant X3	XM_047416695.1:c.456+2577=	XM_047416695.1:c.456+2577C>A
SSBP3 transcript variant X5	XM_047416697.1:c.516+2577=	XM_047416697.1:c.516+2577C>A

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#.

64 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13986094	Dec 05, 2003 (119)
2	HGSV	ss77649024	Dec 06, 2007 (129)
3	HGSV	ss78514999	Dec 06, 2007 (129)
4	BGI	ss102741531	Dec 01, 2009 (131)
5	1000GENOMES	ss108198777	Jan 23, 2009 (130)
6	1000GENOMES	ss110447649	Jan 24, 2009 (130)
7	GMI	ss154995907	Dec 01, 2009 (131)
8	ILLUMINA	ss159867146	Dec 01, 2009 (131)
9	COMPLETE_GENOMICS	ss163387615	Jul 04, 2010 (132)
10	COMPLETE_GENOMICS	ss164281441	Jul 04, 2010 (132)
11	1000GENOMES	ss218381613	Jul 14, 2010 (132)
12	1000GENOMES	ss230531942	Jul 14, 2010 (132)
13	1000GENOMES	ss238226666	Jul 15, 2010 (132)
14	BL	ss253094069	May 09, 2011 (134)
15	GMI	ss275823912	May 04, 2012 (137)
16	ILLUMINA	ss479534900	Sep 08, 2015 (146)
17	TISHKOFF	ss554105788	Apr 25, 2013 (138)
18	SSMP	ss647932617	Apr 25, 2013 (138)
19	EVA-GONL	ss975154108	Aug 21, 2014 (142)
20	JMKIDD_LAB	ss1067881485	Aug 21, 2014 (142)
21	1000GENOMES	ss1290870591	Aug 21, 2014 (142)
22	DDI	ss1425806207	Apr 01, 2015 (144)
23	EVA_GENOME_DK	ss1574054300	Apr 01, 2015 (144)
24	EVA_DECODE	ss1584520215	Apr 01, 2015 (144)
25	EVA_UK10K_ALSPAC	ss1600161546	Apr 01, 2015 (144)
26	EVA_UK10K_TWINSUK	ss1643155579	Apr 01, 2015 (144)
27	WEILL_CORNELL_DGM	ss1918362918	Feb 12, 2016 (147)
28	JJLAB	ss2019696581	Sep 14, 2016 (149)
29	USC_VALOUEV	ss2147710597	Dec 20, 2016 (150)
30	HUMAN_LONGEVITY	ss2162460457	Dec 20, 2016 (150)
31	SYSTEMSBIOZJU	ss2624360980	Nov 08, 2017 (151)
32	GRF	ss2697622398	Nov 08, 2017 (151)
33	GNOMAD	ss2755092080	Nov 08, 2017 (151)
34	SWEGEN	ss2986807951	Nov 08, 2017 (151)
35	BIOINF_KMB_FNS_UNIBA	ss3023608316	Nov 08, 2017 (151)
36	CSHL	ss3343450651	Nov 08, 2017 (151)
37	ILLUMINA	ss3635999641	Oct 11, 2018 (152)
38	EGCUT_WGS	ss3654871774	Jul 12, 2019 (153)
39	EVA_DECODE	ss3686760074	Jul 12, 2019 (153)
40	ACPOP	ss3727041486	Jul 12, 2019 (153)
41	EVA	ss3746196195	Jul 12, 2019 (153)
42	PACBIO	ss3783407082	Jul 12, 2019 (153)
43	PACBIO	ss3789065337	Jul 12, 2019 (153)
44	PACBIO	ss3793938006	Jul 12, 2019 (153)
45	KHV_HUMAN_GENOMES	ss3799205548	Jul 12, 2019 (153)
46	EVA	ss3826168126	Apr 25, 2020 (154)
47	EVA	ss3836470807	Apr 25, 2020 (154)
48	EVA	ss3841876842	Apr 25, 2020 (154)
49	SGDP_PRJ	ss3848834409	Apr 25, 2020 (154)
50	KRGDB	ss3893843149	Apr 25, 2020 (154)
51	KOGIC	ss3944499654	Apr 25, 2020 (154)
52	TOPMED	ss4449562688	Apr 25, 2021 (155)
53	TOMMO_GENOMICS	ss5143925383	Apr 25, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5242249910	Oct 12, 2022 (156)
55	EVA	ss5318689313	Oct 12, 2022 (156)
56	HUGCELL_USP	ss5443313563	Oct 12, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5514517403	Oct 12, 2022 (156)
58	SANFORD_IMAGENETICS	ss5625517510	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5668691160	Oct 12, 2022 (156)
60	YY_MCH	ss5800590230	Oct 12, 2022 (156)
61	EVA	ss5831951093	Oct 12, 2022 (156)
62	EVA	ss5848902325	Oct 12, 2022 (156)
63	EVA	ss5908237162	Oct 12, 2022 (156)
64	EVA	ss5937348812	Oct 12, 2022 (156)
65	1000Genomes	NC_000001.10 - 54702225	Oct 11, 2018 (152)
66	1000Genomes_30x	NC_000001.11 - 54236552	Oct 12, 2022 (156)
67	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 54702225	Oct 11, 2018 (152)
68	Genetic variation in the Estonian population	NC_000001.10 - 54702225	Oct 11, 2018 (152)
69	The Danish reference pan genome	NC_000001.10 - 54702225	Apr 25, 2020 (154)
70	gnomAD - Genomes	NC_000001.11 - 54236552	Apr 25, 2021 (155)
71	Genome of the Netherlands Release 5	NC_000001.10 - 54702225	Apr 25, 2020 (154)
72	HapMap	NC_000001.11 - 54236552	Apr 25, 2020 (154)
73	KOREAN population from KRGDB	NC_000001.10 - 54702225	Apr 25, 2020 (154)
74	Korean Genome Project	NC_000001.11 - 54236552	Apr 25, 2020 (154)
75	Northern Sweden	NC_000001.10 - 54702225	Jul 12, 2019 (153)
76	Qatari	NC_000001.10 - 54702225	Apr 25, 2020 (154)
77	SGDP_PRJ	NC_000001.10 - 54702225	Apr 25, 2020 (154)
78	Siberian	NC_000001.10 - 54702225	Apr 25, 2020 (154)
79	8.3KJPN	NC_000001.10 - 54702225	Apr 25, 2021 (155)
80	14KJPN	NC_000001.11 - 54236552	Oct 12, 2022 (156)
81	TopMed	NC_000001.11 - 54236552	Apr 25, 2021 (155)
82	UK 10K study - Twins	NC_000001.10 - 54702225	Oct 11, 2018 (152)
83	A Vietnamese Genetic Variation Database	NC_000001.10 - 54702225	Jul 12, 2019 (153)
84	ALFA	NC_000001.11 - 54236552	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77649024, ss78514999	NC_000001.8:54414245:G:T	NC_000001.11:54236551:G:T	(self)
ss108198777, ss110447649, ss163387615, ss164281441, ss253094069, ss275823912, ss1584520215	NC_000001.9:54474812:G:T	NC_000001.11:54236551:G:T	(self)
1588156, 863289, 610022, 1498933, 365801, 1020543, 326351, 404848, 851389, 226951, 1894690, 863289, 176727, ss218381613, ss230531942, ss238226666, ss479534900, ss554105788, ss647932617, ss975154108, ss1067881485, ss1290870591, ss1425806207, ss1574054300, ss1600161546, ss1643155579, ss1918362918, ss2019696581, ss2147710597, ss2624360980, ss2697622398, ss2755092080, ss2986807951, ss3343450651, ss3635999641, ss3654871774, ss3727041486, ss3746196195, ss3783407082, ss3789065337, ss3793938006, ss3826168126, ss3836470807, ss3848834409, ss3893843149, ss5143925383, ss5318689313, ss5625517510, ss5831951093, ss5937348812	NC_000001.10:54702224:G:T	NC_000001.11:54236551:G:T	(self)
2043338, 11248132, 67022, 877655, 2528264, 13169023, 9597515532, ss2162460457, ss3023608316, ss3686760074, ss3799205548, ss3841876842, ss3944499654, ss4449562688, ss5242249910, ss5443313563, ss5514517403, ss5668691160, ss5800590230, ss5848902325, ss5908237162	NC_000001.11:54236551:G:T	NC_000001.11:54236551:G:T	(self)
ss13986094	NT_032977.6:16265295:G:T	NC_000001.11:54236551:G:T	(self)
ss102741531, ss154995907, ss159867146	NT_032977.9:24674142:G:T	NC_000001.11:54236551:G:T	(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 rs10127740

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

rs10127740