Name: rs12985777
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.

rs12985777

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:2268056 (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: T>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.363640 (96252/264690, TOPMED)
T=0.256661 (39782/154998, ALFA)
T=0.366191 (51310/140118, GnomAD) (+ 18 more)
T=0.41500 (32659/78696, PAGE_STUDY)
T=0.08154 (2304/28256, 14KJPN)
T=0.08277 (1387/16758, 8.3KJPN)
T=0.3357 (2150/6404, 1000G_30x)
T=0.3213 (1609/5008, 1000G)
T=0.2650 (1187/4480, Estonian)
T=0.2519 (971/3854, ALSPAC)
T=0.2368 (878/3708, TWINSUK)
T=0.1222 (358/2930, KOREAN)
T=0.3925 (741/1888, HapMap)
T=0.1354 (248/1832, Korea1K)
T=0.267 (266/998, GoNL)
T=0.262 (157/600, NorthernSweden)
T=0.139 (69/498, SGDP_PRJ)
T=0.236 (51/216, Qatari)
T=0.060 (13/216, Vietnamese)
T=0.20 (11/54, Siberian)
T=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: OAZ1 : 2KB Upstream Variant
LOC105372240 : 500B Downstream 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	154998	T=0.256661	A=0.000000, C=0.743339, G=0.000000
European	Sub	127656	T=0.222912	A=0.000000, C=0.777088, G=0.000000
African	Sub	10128	T=0.69105	A=0.00000, C=0.30895, G=0.00000
African Others	Sub	322	T=0.776	A=0.000, C=0.224, G=0.000
African American	Sub	9806	T=0.6883	A=0.0000, C=0.3117, G=0.0000
Asian	Sub	710	T=0.082	A=0.000, C=0.918, G=0.000
East Asian	Sub	548	T=0.084	A=0.000, C=0.916, G=0.000
Other Asian	Sub	162	T=0.074	A=0.000, C=0.926, G=0.000
Latin American 1	Sub	896	T=0.339	A=0.000, C=0.661, G=0.000
Latin American 2	Sub	8472	T=0.2485	A=0.0000, C=0.7515, G=0.0000
South Asian	Sub	202	T=0.213	A=0.000, C=0.787, G=0.000
Other	Sub	6934	T=0.2620	A=0.0000, C=0.7380, G=0.0000

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	T=0.363640	C=0.636360
Allele Frequency Aggregator	Total	Global	154998	T=0.256661	A=0.000000, C=0.743339, G=0.000000
Allele Frequency Aggregator	European	Sub	127656	T=0.222912	A=0.000000, C=0.777088, G=0.000000
Allele Frequency Aggregator	African	Sub	10128	T=0.69105	A=0.00000, C=0.30895, G=0.00000
Allele Frequency Aggregator	Latin American 2	Sub	8472	T=0.2485	A=0.0000, C=0.7515, G=0.0000
Allele Frequency Aggregator	Other	Sub	6934	T=0.2620	A=0.0000, C=0.7380, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	896	T=0.339	A=0.000, C=0.661, G=0.000
Allele Frequency Aggregator	Asian	Sub	710	T=0.082	A=0.000, C=0.918, G=0.000
Allele Frequency Aggregator	South Asian	Sub	202	T=0.213	A=0.000, C=0.787, G=0.000
gnomAD - Genomes	Global	Study-wide	140118	T=0.366191	C=0.633809
gnomAD - Genomes	European	Sub	75878	T=0.24079	C=0.75921
gnomAD - Genomes	African	Sub	41994	T=0.68322	C=0.31678
gnomAD - Genomes	American	Sub	13650	T=0.22007	C=0.77993
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.1315	C=0.8685
gnomAD - Genomes	East Asian	Sub	3124	T=0.0835	C=0.9165
gnomAD - Genomes	Other	Sub	2148	T=0.3007	C=0.6993
The PAGE Study	Global	Study-wide	78696	T=0.41500	C=0.58500
The PAGE Study	AfricanAmerican	Sub	32512	T=0.66877	C=0.33123
The PAGE Study	Mexican	Sub	10810	T=0.27983	C=0.72017
The PAGE Study	Asian	Sub	8316	T=0.0903	C=0.9097
The PAGE Study	PuertoRican	Sub	7918	T=0.2834	C=0.7166
The PAGE Study	NativeHawaiian	Sub	4534	T=0.0926	C=0.9074
The PAGE Study	Cuban	Sub	4230	T=0.2693	C=0.7307
The PAGE Study	Dominican	Sub	3828	T=0.4483	C=0.5517
The PAGE Study	CentralAmerican	Sub	2450	T=0.2645	C=0.7355
The PAGE Study	SouthAmerican	Sub	1982	T=0.2043	C=0.7957
The PAGE Study	NativeAmerican	Sub	1260	T=0.3294	C=0.6706
The PAGE Study	SouthAsian	Sub	856	T=0.179	C=0.821
14KJPN	JAPANESE	Study-wide	28256	T=0.08154	C=0.91846
8.3KJPN	JAPANESE	Study-wide	16758	T=0.08277	C=0.91723
1000Genomes_30x	Global	Study-wide	6404	T=0.3357	C=0.6643
1000Genomes_30x	African	Sub	1786	T=0.7699	C=0.2301
1000Genomes_30x	Europe	Sub	1266	T=0.2204	C=0.7796
1000Genomes_30x	South Asian	Sub	1202	T=0.1747	C=0.8253
1000Genomes_30x	East Asian	Sub	1170	T=0.0752	C=0.9248
1000Genomes_30x	American	Sub	980	T=0.202	C=0.798
1000Genomes	Global	Study-wide	5008	T=0.3213	C=0.6787
1000Genomes	African	Sub	1322	T=0.7678	C=0.2322
1000Genomes	East Asian	Sub	1008	T=0.0794	C=0.9206
1000Genomes	Europe	Sub	1006	T=0.2097	C=0.7903
1000Genomes	South Asian	Sub	978	T=0.171	C=0.829
1000Genomes	American	Sub	694	T=0.196	C=0.804
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.2650	C=0.7350
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.2519	C=0.7481
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.2368	C=0.7632
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.1222	C=0.8778, G=0.0000
HapMap	Global	Study-wide	1888	T=0.3925	C=0.6075
HapMap	American	Sub	770	T=0.270	C=0.730
HapMap	African	Sub	688	T=0.693	C=0.307
HapMap	Asian	Sub	254	T=0.106	C=0.894
HapMap	Europe	Sub	176	T=0.165	C=0.835
Korean Genome Project	KOREAN	Study-wide	1832	T=0.1354	C=0.8646
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.267	C=0.733
Northern Sweden	ACPOP	Study-wide	600	T=0.262	C=0.738
SGDP_PRJ	Global	Study-wide	498	T=0.139	C=0.861
Qatari	Global	Study-wide	216	T=0.236	C=0.764
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.060	C=0.940
Siberian	Global	Study-wide	54	T=0.20	C=0.80
The Danish reference pan genome	Danish	Study-wide	40	T=0.20	C=0.80

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 19	NC_000019.10:g.2268056T>A
GRCh38.p14 chr 19	NC_000019.10:g.2268056T>C
GRCh38.p14 chr 19	NC_000019.10:g.2268056T>G
GRCh37.p13 chr 19	NC_000019.9:g.2268055T>A
GRCh37.p13 chr 19	NC_000019.9:g.2268055T>C
GRCh37.p13 chr 19	NC_000019.9:g.2268055T>G

Gene: OAZ1, ornithine decarboxylase antizyme 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
OAZ1 transcript variant 2	NM_001301020.1:c.	N/A	Upstream Transcript Variant
OAZ1 transcript variant 1	NM_004152.3:c.	N/A	Upstream Transcript Variant

Gene: LOC105372240, uncharacterized LOC105372240 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105372240 transcript	XR_936242.3:n.	N/A	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	T=	A	C	G
GRCh38.p14 chr 19	NC_000019.10:g.2268056=	NC_000019.10:g.2268056T>A	NC_000019.10:g.2268056T>C	NC_000019.10:g.2268056T>G
GRCh37.p13 chr 19	NC_000019.9:g.2268055=	NC_000019.9:g.2268055T>A	NC_000019.9:g.2268055T>C	NC_000019.9:g.2268055T>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#.

121 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSAHASNP	ss21555711	Apr 05, 2004 (121)
2	EGP_SNPS	ss32479327	May 24, 2005 (125)
3	AFFY	ss66093226	Nov 29, 2006 (127)
4	EGP_SNPS	ss66857574	Nov 29, 2006 (127)
5	PERLEGEN	ss69222386	May 17, 2007 (127)
6	ILLUMINA	ss75017999	Dec 06, 2007 (129)
7	AFFY	ss76050069	Dec 08, 2007 (129)
8	HGSV	ss77543005	Dec 06, 2007 (129)
9	KRIBB_YJKIM	ss83026483	Dec 15, 2007 (130)
10	HGSV	ss83185224	Dec 14, 2007 (130)
11	HGSV	ss83487329	Dec 14, 2007 (130)
12	HUMANGENOME_JCVI	ss96249117	Feb 04, 2009 (130)
13	BGI	ss103418171	Dec 01, 2009 (131)
14	1000GENOMES	ss110984680	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss117618084	Feb 14, 2009 (130)
16	ENSEMBL	ss136301878	Dec 01, 2009 (131)
17	GMI	ss155528548	Dec 01, 2009 (131)
18	ILLUMINA	ss160310878	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss167661542	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss171390375	Jul 04, 2010 (132)
21	ILLUMINA	ss172296318	Jul 04, 2010 (132)
22	AFFY	ss172322109	Jul 04, 2010 (132)
23	BUSHMAN	ss203590934	Jul 04, 2010 (132)
24	BCM-HGSC-SUB	ss208433467	Jul 04, 2010 (132)
25	1000GENOMES	ss228009727	Jul 14, 2010 (132)
26	1000GENOMES	ss237579041	Jul 15, 2010 (132)
27	1000GENOMES	ss243806202	Jul 15, 2010 (132)
28	BL	ss255434532	May 09, 2011 (134)
29	GMI	ss283098525	May 04, 2012 (137)
30	GMI	ss287333895	Apr 25, 2013 (138)
31	PJP	ss292173855	May 09, 2011 (134)
32	ILLUMINA	ss479853165	May 04, 2012 (137)
33	ILLUMINA	ss479860750	May 04, 2012 (137)
34	ILLUMINA	ss480460180	Sep 08, 2015 (146)
35	ILLUMINA	ss484725095	May 04, 2012 (137)
36	ILLUMINA	ss536826149	Sep 08, 2015 (146)
37	TISHKOFF	ss565810242	Apr 25, 2013 (138)
38	SSMP	ss661662748	Apr 25, 2013 (138)
39	ILLUMINA	ss778419179	Sep 08, 2015 (146)
40	ILLUMINA	ss782809248	Sep 08, 2015 (146)
41	ILLUMINA	ss783774525	Sep 08, 2015 (146)
42	ILLUMINA	ss832062398	Sep 08, 2015 (146)
43	ILLUMINA	ss833874526	Sep 08, 2015 (146)
44	EVA-GONL	ss994015939	Aug 21, 2014 (142)
45	JMKIDD_LAB	ss1081713282	Aug 21, 2014 (142)
46	1000GENOMES	ss1362080966	Aug 21, 2014 (142)
47	DDI	ss1428312506	Apr 01, 2015 (144)
48	EVA_GENOME_DK	ss1578526867	Apr 01, 2015 (144)
49	EVA_UK10K_ALSPAC	ss1637438261	Apr 01, 2015 (144)
50	EVA_UK10K_TWINSUK	ss1680432294	Apr 01, 2015 (144)
51	EVA_DECODE	ss1698078904	Apr 01, 2015 (144)
52	EVA_SVP	ss1713646909	Apr 01, 2015 (144)
53	ILLUMINA	ss1752278821	Sep 08, 2015 (146)
54	HAMMER_LAB	ss1809174429	Sep 08, 2015 (146)
55	WEILL_CORNELL_DGM	ss1937493072	Feb 12, 2016 (147)
56	ILLUMINA	ss1959828545	Feb 12, 2016 (147)
57	GENOMED	ss1968593164	Jul 19, 2016 (147)
58	JJLAB	ss2029521609	Sep 14, 2016 (149)
59	ILLUMINA	ss2094803391	Dec 20, 2016 (150)
60	ILLUMINA	ss2095082763	Dec 20, 2016 (150)
61	USC_VALOUEV	ss2158034464	Dec 20, 2016 (150)
62	HUMAN_LONGEVITY	ss2223742107	Dec 20, 2016 (150)
63	SYSTEMSBIOZJU	ss2629259425	Nov 08, 2017 (151)
64	ILLUMINA	ss2633509398	Nov 08, 2017 (151)
65	ILLUMINA	ss2635080874	Nov 08, 2017 (151)
66	GRF	ss2702637993	Nov 08, 2017 (151)
67	GNOMAD	ss2959656295	Nov 08, 2017 (151)
68	AFFY	ss2985764130	Nov 08, 2017 (151)
69	SWEGEN	ss3016968875	Nov 08, 2017 (151)
70	ILLUMINA	ss3021869168	Nov 08, 2017 (151)
71	BIOINF_KMB_FNS_UNIBA	ss3028593190	Nov 08, 2017 (151)
72	CSHL	ss3352162063	Nov 08, 2017 (151)
73	ILLUMINA	ss3627872323	Oct 12, 2018 (152)
74	ILLUMINA	ss3631483646	Oct 12, 2018 (152)
75	ILLUMINA	ss3633172468	Oct 12, 2018 (152)
76	ILLUMINA	ss3633881896	Oct 12, 2018 (152)
77	ILLUMINA	ss3634718756	Oct 12, 2018 (152)
78	ILLUMINA	ss3635568958	Oct 12, 2018 (152)
79	ILLUMINA	ss3636409335	Oct 12, 2018 (152)
80	ILLUMINA	ss3637320626	Oct 12, 2018 (152)
81	ILLUMINA	ss3638211477	Oct 12, 2018 (152)
82	ILLUMINA	ss3640426064	Oct 12, 2018 (152)
83	ILLUMINA	ss3643186091	Oct 12, 2018 (152)
84	URBANLAB	ss3650852911	Oct 12, 2018 (152)
85	ILLUMINA	ss3652293156	Oct 12, 2018 (152)
86	ILLUMINA	ss3652293157	Oct 12, 2018 (152)
87	EGCUT_WGS	ss3683817714	Jul 13, 2019 (153)
88	EVA_DECODE	ss3702195046	Jul 13, 2019 (153)
89	ILLUMINA	ss3725699017	Jul 13, 2019 (153)
90	ACPOP	ss3742790686	Jul 13, 2019 (153)
91	ILLUMINA	ss3745018827	Jul 13, 2019 (153)
92	EVA	ss3755727824	Jul 13, 2019 (153)
93	PAGE_CC	ss3771989785	Jul 13, 2019 (153)
94	ILLUMINA	ss3772516244	Jul 13, 2019 (153)
95	PACBIO	ss3788447337	Jul 13, 2019 (153)
96	PACBIO	ss3793370583	Jul 13, 2019 (153)
97	PACBIO	ss3798257130	Jul 13, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3820981260	Jul 13, 2019 (153)
99	EVA	ss3835312363	Apr 27, 2020 (154)
100	EVA	ss3841278658	Apr 27, 2020 (154)
101	EVA	ss3846782520	Apr 27, 2020 (154)
102	SGDP_PRJ	ss3887602728	Apr 27, 2020 (154)
103	KRGDB	ss3937533362	Apr 27, 2020 (154)
104	KOGIC	ss3980660464	Apr 27, 2020 (154)
105	TOPMED	ss5065760424	Apr 26, 2021 (155)
106	TOMMO_GENOMICS	ss5226383072	Apr 26, 2021 (155)
107	1000G_HIGH_COVERAGE	ss5306230541	Oct 16, 2022 (156)
108	EVA	ss5315956284	Oct 16, 2022 (156)
109	EVA	ss5433128699	Oct 16, 2022 (156)
110	HUGCELL_USP	ss5498899365	Oct 16, 2022 (156)
111	EVA	ss5512028365	Oct 16, 2022 (156)
112	1000G_HIGH_COVERAGE	ss5611530805	Oct 16, 2022 (156)
113	SANFORD_IMAGENETICS	ss5661834651	Oct 16, 2022 (156)
114	TOMMO_GENOMICS	ss5784535401	Oct 16, 2022 (156)
115	EVA	ss5800002068	Oct 16, 2022 (156)
116	YY_MCH	ss5817341941	Oct 16, 2022 (156)
117	EVA	ss5840153952	Oct 16, 2022 (156)
118	EVA	ss5852175827	Oct 16, 2022 (156)
119	EVA	ss5927027580	Oct 16, 2022 (156)
120	EVA	ss5953265315	Oct 16, 2022 (156)
121	EVA	ss5981023615	Oct 16, 2022 (156)
122	1000Genomes	NC_000019.9 - 2268055	Oct 12, 2018 (152)
123	1000Genomes_30x	NC_000019.10 - 2268056	Oct 16, 2022 (156)
124	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 2268055	Oct 12, 2018 (152)
125	Genetic variation in the Estonian population	NC_000019.9 - 2268055	Oct 12, 2018 (152)
126	The Danish reference pan genome	NC_000019.9 - 2268055	Apr 27, 2020 (154)
127	gnomAD - Genomes	NC_000019.10 - 2268056	Apr 26, 2021 (155)
128	Genome of the Netherlands Release 5	NC_000019.9 - 2268055	Apr 27, 2020 (154)
129	HapMap	NC_000019.10 - 2268056	Apr 27, 2020 (154)
130	KOREAN population from KRGDB	NC_000019.9 - 2268055	Apr 27, 2020 (154)
131	Korean Genome Project	NC_000019.10 - 2268056	Apr 27, 2020 (154)
132	Northern Sweden	NC_000019.9 - 2268055	Jul 13, 2019 (153)
133	The PAGE Study	NC_000019.10 - 2268056	Jul 13, 2019 (153)
134	Qatari	NC_000019.9 - 2268055	Apr 27, 2020 (154)
135	SGDP_PRJ	NC_000019.9 - 2268055	Apr 27, 2020 (154)
136	Siberian	NC_000019.9 - 2268055	Apr 27, 2020 (154)
137	8.3KJPN	NC_000019.9 - 2268055	Apr 26, 2021 (155)
138	14KJPN	NC_000019.10 - 2268056	Oct 16, 2022 (156)
139	TopMed	NC_000019.10 - 2268056	Apr 26, 2021 (155)
140	UK 10K study - Twins	NC_000019.9 - 2268055	Oct 12, 2018 (152)
141	A Vietnamese Genetic Variation Database	NC_000019.9 - 2268055	Jul 13, 2019 (153)
142	ALFA	NC_000019.10 - 2268056	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)
rs57201072	May 23, 2008 (130)
rs59919871	Feb 26, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
10175510603	NC_000019.10:2268055:T:A	NC_000019.10:2268055:T:A	(self)
ss66093226, ss76050069, ss77543005, ss83185224, ss83487329, ss110984680, ss117618084, ss167661542, ss171390375, ss172322109, ss203590934, ss208433467, ss255434532, ss283098525, ss287333895, ss292173855, ss479853165, ss1698078904, ss1713646909, ss2635080874, ss3643186091	NC_000019.8:2219054:T:C	NC_000019.10:2268055:T:C	(self)
75447774, 41817897, 29555962, 4713975, 18630844, 44710756, 16075551, 19534994, 39619708, 10550818, 84352379, 41817897, 9247728, ss228009727, ss237579041, ss243806202, ss479860750, ss480460180, ss484725095, ss536826149, ss565810242, ss661662748, ss778419179, ss782809248, ss783774525, ss832062398, ss833874526, ss994015939, ss1081713282, ss1362080966, ss1428312506, ss1578526867, ss1637438261, ss1680432294, ss1752278821, ss1809174429, ss1937493072, ss1959828545, ss1968593164, ss2029521609, ss2094803391, ss2095082763, ss2158034464, ss2629259425, ss2633509398, ss2702637993, ss2959656295, ss2985764130, ss3016968875, ss3021869168, ss3352162063, ss3627872323, ss3631483646, ss3633172468, ss3633881896, ss3634718756, ss3635568958, ss3636409335, ss3637320626, ss3638211477, ss3640426064, ss3652293156, ss3652293157, ss3683817714, ss3742790686, ss3745018827, ss3755727824, ss3772516244, ss3788447337, ss3793370583, ss3798257130, ss3835312363, ss3841278658, ss3887602728, ss3937533362, ss5226383072, ss5315956284, ss5433128699, ss5512028365, ss5661834651, ss5800002068, ss5840153952, ss5953265315, ss5981023615	NC_000019.9:2268054:T:C	NC_000019.10:2268055:T:C	(self)
99056740, 532073029, 1659071, 37038465, 1211254, 118372505, 281306088, 10175510603, ss2223742107, ss3028593190, ss3650852911, ss3702195046, ss3725699017, ss3771989785, ss3820981260, ss3846782520, ss3980660464, ss5065760424, ss5306230541, ss5498899365, ss5611530805, ss5784535401, ss5817341941, ss5852175827, ss5927027580	NC_000019.10:2268055:T:C	NC_000019.10:2268055:T:C	(self)
ss21555711, ss32479327, ss66857574, ss69222386, ss75017999, ss83026483, ss96249117, ss103418171, ss136301878, ss155528548, ss160310878, ss172296318	NT_011255.14:2208054:T:C	NC_000019.10:2268055:T:C	(self)
44710756, ss3937533362	NC_000019.9:2268054:T:G	NC_000019.10:2268055:T:G	(self)
10175510603	NC_000019.10:2268055:T:G	NC_000019.10:2268055:T: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 rs12985777

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
Top▲ Help
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

rs12985777