Name: rs17612678
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.

rs17612678

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:93271900 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.266244 (70472/264690, TOPMED)
C=0.377568 (96810/256404, ALFA)
C=0.288075 (40315/139946, GnomAD) (+ 23 more)
C=0.15814 (12445/78696, PAGE_STUDY)
C=0.03882 (1097/28258, 14KJPN)
C=0.03950 (662/16760, 8.3KJPN)
C=0.1783 (1142/6404, 1000G_30x)
C=0.1773 (888/5008, 1000G)
C=0.3944 (1767/4480, Estonian)
C=0.4043 (1558/3854, ALSPAC)
C=0.4199 (1557/3708, TWINSUK)
C=0.0469 (137/2922, KOREAN)
C=0.2044 (426/2084, HGDP_Stanford)
C=0.0508 (93/1832, Korea1K)
C=0.1667 (265/1590, HapMap)
C=0.3686 (418/1134, Daghestan)
C=0.418 (417/998, GoNL)
C=0.045 (36/792, PRJEB37584)
C=0.268 (168/626, Chileans)
C=0.460 (276/600, NorthernSweden)
C=0.227 (49/216, Qatari)
C=0.061 (13/212, Vietnamese)
T=0.425 (79/186, SGDP_PRJ)
T=0.49 (44/90, Ancient Sardinia)
C=0.47 (19/40, GENOME_DK)
T=0.36 (13/36, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC105370982 : 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	256404	T=0.622432	C=0.377568
European	Sub	225844	T=0.594871	C=0.405129
African	Sub	11192	T=0.93120	C=0.06880
African Others	Sub	390	T=0.992	C=0.008
African American	Sub	10802	T=0.92899	C=0.07101
Asian	Sub	3910	T=0.9665	C=0.0335
East Asian	Sub	3148	T=0.9647	C=0.0353
Other Asian	Sub	762	T=0.974	C=0.026
Latin American 1	Sub	1116	T=0.7213	C=0.2787
Latin American 2	Sub	4698	T=0.7380	C=0.2620
South Asian	Sub	380	T=0.732	C=0.268
Other	Sub	9264	T=0.7011	C=0.2989

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	T=0.733756	C=0.266244
Allele Frequency Aggregator	Total	Global	256404	T=0.622432	C=0.377568
Allele Frequency Aggregator	European	Sub	225844	T=0.594871	C=0.405129
Allele Frequency Aggregator	African	Sub	11192	T=0.93120	C=0.06880
Allele Frequency Aggregator	Other	Sub	9264	T=0.7011	C=0.2989
Allele Frequency Aggregator	Latin American 2	Sub	4698	T=0.7380	C=0.2620
Allele Frequency Aggregator	Asian	Sub	3910	T=0.9665	C=0.0335
Allele Frequency Aggregator	Latin American 1	Sub	1116	T=0.7213	C=0.2787
Allele Frequency Aggregator	South Asian	Sub	380	T=0.732	C=0.268
gnomAD - Genomes	Global	Study-wide	139946	T=0.711925	C=0.288075
gnomAD - Genomes	European	Sub	75780	T=0.58655	C=0.41345
gnomAD - Genomes	African	Sub	41946	T=0.92447	C=0.07553
gnomAD - Genomes	American	Sub	13622	T=0.70812	C=0.29188
gnomAD - Genomes	Ashkenazi Jewish	Sub	3316	T=0.6616	C=0.3384
gnomAD - Genomes	East Asian	Sub	3130	T=0.9604	C=0.0396
gnomAD - Genomes	Other	Sub	2152	T=0.7240	C=0.2760
The PAGE Study	Global	Study-wide	78696	T=0.84186	C=0.15814
The PAGE Study	AfricanAmerican	Sub	32510	T=0.91941	C=0.08059
The PAGE Study	Mexican	Sub	10810	T=0.74107	C=0.25893
The PAGE Study	Asian	Sub	8318	T=0.9636	C=0.0364
The PAGE Study	PuertoRican	Sub	7918	T=0.7054	C=0.2946
The PAGE Study	NativeHawaiian	Sub	4534	T=0.8663	C=0.1337
The PAGE Study	Cuban	Sub	4230	T=0.6747	C=0.3253
The PAGE Study	Dominican	Sub	3828	T=0.7913	C=0.2087
The PAGE Study	CentralAmerican	Sub	2450	T=0.7804	C=0.2196
The PAGE Study	SouthAmerican	Sub	1982	T=0.7467	C=0.2533
The PAGE Study	NativeAmerican	Sub	1260	T=0.7000	C=0.3000
The PAGE Study	SouthAsian	Sub	856	T=0.777	C=0.223
14KJPN	JAPANESE	Study-wide	28258	T=0.96118	C=0.03882
8.3KJPN	JAPANESE	Study-wide	16760	T=0.96050	C=0.03950
1000Genomes_30x	Global	Study-wide	6404	T=0.8217	C=0.1783
1000Genomes_30x	African	Sub	1786	T=0.9815	C=0.0185
1000Genomes_30x	Europe	Sub	1266	T=0.5782	C=0.4218
1000Genomes_30x	South Asian	Sub	1202	T=0.8020	C=0.1980
1000Genomes_30x	East Asian	Sub	1170	T=0.9547	C=0.0453
1000Genomes_30x	American	Sub	980	T=0.710	C=0.290
1000Genomes	Global	Study-wide	5008	T=0.8227	C=0.1773
1000Genomes	African	Sub	1322	T=0.9766	C=0.0234
1000Genomes	East Asian	Sub	1008	T=0.9563	C=0.0437
1000Genomes	Europe	Sub	1006	T=0.5865	C=0.4135
1000Genomes	South Asian	Sub	978	T=0.803	C=0.197
1000Genomes	American	Sub	694	T=0.706	C=0.294
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6056	C=0.3944
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5957	C=0.4043
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5801	C=0.4199
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.9531	C=0.0469
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.7956	C=0.2044
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.921	C=0.079
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.715	C=0.285
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.760	C=0.240
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.550	C=0.450
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.996	C=0.004
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.810	C=0.190
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.99	C=0.01
Korean Genome Project	KOREAN	Study-wide	1832	T=0.9492	C=0.0508
HapMap	Global	Study-wide	1590	T=0.8333	C=0.1667
HapMap	American	Sub	768	T=0.767	C=0.233
HapMap	African	Sub	394	T=0.992	C=0.008
HapMap	Asian	Sub	252	T=0.964	C=0.036
HapMap	Europe	Sub	176	T=0.580	C=0.420
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	T=0.6314	C=0.3686
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	T=0.596	C=0.404
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.688	C=0.312
Genome-wide autozygosity in Daghestan	Central Asia	Sub	120	T=0.700	C=0.300
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.519	C=0.481
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.82	C=0.18
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.64	C=0.36
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.582	C=0.418
CNV burdens in cranial meningiomas	Global	Study-wide	792	T=0.955	C=0.045
CNV burdens in cranial meningiomas	CRM	Sub	792	T=0.955	C=0.045
Chileans	Chilean	Study-wide	626	T=0.732	C=0.268
Northern Sweden	ACPOP	Study-wide	600	T=0.540	C=0.460
Qatari	Global	Study-wide	216	T=0.773	C=0.227
A Vietnamese Genetic Variation Database	Global	Study-wide	212	T=0.939	C=0.061
SGDP_PRJ	Global	Study-wide	186	T=0.425	C=0.575
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	90	T=0.49	C=0.51
The Danish reference pan genome	Danish	Study-wide	40	T=0.53	C=0.47
Siberian	Global	Study-wide	36	T=0.36	C=0.64

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 15	NC_000015.10:g.93271900T>C
GRCh37.p13 chr 15	NC_000015.9:g.93815129T>C

Gene: LOC105370982, uncharacterized LOC105370982 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105370982 transcript	XR_007064770.1:n.	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	T=	C
GRCh38.p14 chr 15	NC_000015.10:g.93271900=	NC_000015.10:g.93271900T>C
GRCh37.p13 chr 15	NC_000015.9:g.93815129=	NC_000015.9:g.93815129T>C

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#.

119 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss24668093	Sep 20, 2004 (123)
2	AFFY	ss66217554	Nov 30, 2006 (127)
3	ILLUMINA	ss66772558	Nov 30, 2006 (127)
4	ILLUMINA	ss67189683	Nov 30, 2006 (127)
5	ILLUMINA	ss67569034	Nov 30, 2006 (127)
6	PERLEGEN	ss69185636	May 17, 2007 (127)
7	ILLUMINA	ss70667811	May 24, 2008 (130)
8	ILLUMINA	ss71229789	May 17, 2007 (127)
9	ILLUMINA	ss75750957	Dec 06, 2007 (129)
10	AFFY	ss76364050	Dec 06, 2007 (129)
11	ILLUMINA	ss79092011	Dec 15, 2007 (130)
12	KRIBB_YJKIM	ss85394119	Dec 15, 2007 (130)
13	1000GENOMES	ss109048150	Jan 23, 2009 (130)
14	ILLUMINA	ss121802051	Dec 01, 2009 (131)
15	ILLUMINA	ss160449699	Dec 01, 2009 (131)
16	COMPLETE_GENOMICS	ss168511209	Jul 04, 2010 (132)
17	ILLUMINA	ss172859865	Jul 04, 2010 (132)
18	AFFY	ss173388422	Jul 04, 2010 (132)
19	BCM-HGSC-SUB	ss207327981	Jul 04, 2010 (132)
20	1000GENOMES	ss236884962	Jul 15, 2010 (132)
21	BL	ss255211980	May 09, 2011 (134)
22	GMI	ss287004501	Apr 25, 2013 (138)
23	ILLUMINA	ss480259628	May 04, 2012 (137)
24	ILLUMINA	ss480270471	May 04, 2012 (137)
25	ILLUMINA	ss481014780	Sep 08, 2015 (146)
26	ILLUMINA	ss484927721	May 04, 2012 (137)
27	ILLUMINA	ss536976347	Sep 08, 2015 (146)
28	SSMP	ss660404423	Apr 25, 2013 (138)
29	ILLUMINA	ss778463276	Sep 08, 2015 (146)
30	ILLUMINA	ss782910179	Sep 08, 2015 (146)
31	ILLUMINA	ss783873395	Sep 08, 2015 (146)
32	ILLUMINA	ss825422529	Apr 01, 2015 (144)
33	ILLUMINA	ss832165112	Sep 08, 2015 (146)
34	ILLUMINA	ss833918996	Sep 08, 2015 (146)
35	EVA-GONL	ss992097001	Aug 21, 2014 (142)
36	JMKIDD_LAB	ss1080351071	Aug 21, 2014 (142)
37	1000GENOMES	ss1354670718	Aug 21, 2014 (142)
38	HAMMER_LAB	ss1397705280	Sep 08, 2015 (146)
39	DDI	ss1427720536	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1577758196	Apr 01, 2015 (144)
41	EVA_UK10K_ALSPAC	ss1633643162	Apr 01, 2015 (144)
42	EVA_UK10K_TWINSUK	ss1676637195	Apr 01, 2015 (144)
43	EVA_DECODE	ss1696127030	Apr 01, 2015 (144)
44	EVA_SVP	ss1713512686	Apr 01, 2015 (144)
45	ILLUMINA	ss1752178458	Sep 08, 2015 (146)
46	WEILL_CORNELL_DGM	ss1935500007	Feb 12, 2016 (147)
47	ILLUMINA	ss1946402996	Feb 12, 2016 (147)
48	ILLUMINA	ss1959639565	Feb 12, 2016 (147)
49	GENOMED	ss1968177770	Jul 19, 2016 (147)
50	JJLAB	ss2028533942	Sep 14, 2016 (149)
51	USC_VALOUEV	ss2156943271	Nov 08, 2017 (151)
52	HUMAN_LONGEVITY	ss2209219419	Dec 20, 2016 (150)
53	SYSTEMSBIOZJU	ss2628762014	Nov 08, 2017 (151)
54	ILLUMINA	ss2633269311	Nov 08, 2017 (151)
55	GRF	ss2701431282	Nov 08, 2017 (151)
56	ILLUMINA	ss2710823944	Nov 08, 2017 (151)
57	GNOMAD	ss2938353075	Nov 08, 2017 (151)
58	AFFY	ss2985692188	Nov 08, 2017 (151)
59	SWEGEN	ss3013775526	Nov 08, 2017 (151)
60	ILLUMINA	ss3021663130	Nov 08, 2017 (151)
61	BIOINF_KMB_FNS_UNIBA	ss3028091185	Nov 08, 2017 (151)
62	CSHL	ss3351249688	Nov 08, 2017 (151)
63	ILLUMINA	ss3625681615	Oct 12, 2018 (152)
64	ILLUMINA	ss3627434410	Oct 12, 2018 (152)
65	ILLUMINA	ss3631259447	Oct 12, 2018 (152)
66	ILLUMINA	ss3633107799	Oct 12, 2018 (152)
67	ILLUMINA	ss3633812930	Oct 12, 2018 (152)
68	ILLUMINA	ss3634622132	Oct 12, 2018 (152)
69	ILLUMINA	ss3635501601	Oct 12, 2018 (152)
70	ILLUMINA	ss3636312699	Oct 12, 2018 (152)
71	ILLUMINA	ss3637252930	Oct 12, 2018 (152)
72	ILLUMINA	ss3638103459	Oct 12, 2018 (152)
73	ILLUMINA	ss3639064200	Oct 12, 2018 (152)
74	ILLUMINA	ss3639537783	Oct 12, 2018 (152)
75	ILLUMINA	ss3640329452	Oct 12, 2018 (152)
76	ILLUMINA	ss3641065414	Oct 12, 2018 (152)
77	ILLUMINA	ss3641360865	Oct 12, 2018 (152)
78	ILLUMINA	ss3643086339	Oct 12, 2018 (152)
79	ILLUMINA	ss3644656110	Oct 12, 2018 (152)
80	ILLUMINA	ss3652066131	Oct 12, 2018 (152)
81	EGCUT_WGS	ss3680905944	Jul 13, 2019 (153)
82	EVA_DECODE	ss3698488540	Jul 13, 2019 (153)
83	ILLUMINA	ss3725526640	Jul 13, 2019 (153)
84	ACPOP	ss3741181677	Jul 13, 2019 (153)
85	ILLUMINA	ss3744135629	Jul 13, 2019 (153)
86	ILLUMINA	ss3744922652	Jul 13, 2019 (153)
87	EVA	ss3753463458	Jul 13, 2019 (153)
88	PAGE_CC	ss3771851947	Jul 13, 2019 (153)
89	ILLUMINA	ss3772421131	Jul 13, 2019 (153)
90	KHV_HUMAN_GENOMES	ss3818764962	Jul 13, 2019 (153)
91	EVA	ss3834383633	Apr 27, 2020 (154)
92	EVA	ss3840794650	Apr 27, 2020 (154)
93	EVA	ss3846284842	Apr 27, 2020 (154)
94	HGDP	ss3847533543	Apr 27, 2020 (154)
95	SGDP_PRJ	ss3883555150	Apr 27, 2020 (154)
96	KRGDB	ss3932810211	Apr 27, 2020 (154)
97	KOGIC	ss3976768661	Apr 27, 2020 (154)
98	EVA	ss3984706471	Apr 26, 2021 (155)
99	EVA	ss3985735392	Apr 26, 2021 (155)
100	EVA	ss4017717684	Apr 26, 2021 (155)
101	TOPMED	ss5001922259	Apr 26, 2021 (155)
102	TOMMO_GENOMICS	ss5217607927	Apr 26, 2021 (155)
103	EVA	ss5237556418	Apr 26, 2021 (155)
104	1000G_HIGH_COVERAGE	ss5299506262	Oct 16, 2022 (156)
105	EVA	ss5315808079	Oct 16, 2022 (156)
106	EVA	ss5421177894	Oct 16, 2022 (156)
107	HUGCELL_USP	ss5493112752	Oct 16, 2022 (156)
108	EVA	ss5511524074	Oct 16, 2022 (156)
109	1000G_HIGH_COVERAGE	ss5601436562	Oct 16, 2022 (156)
110	SANFORD_IMAGENETICS	ss5624369189	Oct 16, 2022 (156)
111	SANFORD_IMAGENETICS	ss5658108106	Oct 16, 2022 (156)
112	TOMMO_GENOMICS	ss5771841927	Oct 16, 2022 (156)
113	EVA	ss5799946755	Oct 16, 2022 (156)
114	YY_MCH	ss5815600670	Oct 16, 2022 (156)
115	EVA	ss5828611803	Oct 16, 2022 (156)
116	EVA	ss5847755348	Oct 16, 2022 (156)
117	EVA	ss5877091567	Oct 16, 2022 (156)
118	EVA	ss5949533707	Oct 16, 2022 (156)
119	EVA	ss5979471646	Oct 16, 2022 (156)
120	1000Genomes	NC_000015.9 - 93815129	Oct 12, 2018 (152)
121	1000Genomes_30x	NC_000015.10 - 93271900	Oct 16, 2022 (156)
122	The Avon Longitudinal Study of Parents and Children	NC_000015.9 - 93815129	Oct 12, 2018 (152)
123	Chileans	NC_000015.9 - 93815129	Apr 27, 2020 (154)
124	Genome-wide autozygosity in Daghestan	NC_000015.8 - 91616133	Apr 27, 2020 (154)
125	Genetic variation in the Estonian population	NC_000015.9 - 93815129	Oct 12, 2018 (152)
126	The Danish reference pan genome	NC_000015.9 - 93815129	Apr 27, 2020 (154)
127	gnomAD - Genomes	NC_000015.10 - 93271900	Apr 26, 2021 (155)
128	Genome of the Netherlands Release 5	NC_000015.9 - 93815129	Apr 27, 2020 (154)
129	HGDP-CEPH-db Supplement 1	NC_000015.8 - 91616133	Apr 27, 2020 (154)
130	HapMap	NC_000015.10 - 93271900	Apr 27, 2020 (154)
131	KOREAN population from KRGDB	NC_000015.9 - 93815129	Apr 27, 2020 (154)
132	Korean Genome Project	NC_000015.10 - 93271900	Apr 27, 2020 (154)
133	Northern Sweden	NC_000015.9 - 93815129	Jul 13, 2019 (153)
134	The PAGE Study	NC_000015.10 - 93271900	Jul 13, 2019 (153)
135	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000015.9 - 93815129	Apr 26, 2021 (155)
136	CNV burdens in cranial meningiomas	NC_000015.9 - 93815129	Apr 26, 2021 (155)
137	Qatari	NC_000015.9 - 93815129	Apr 27, 2020 (154)
138	SGDP_PRJ	NC_000015.9 - 93815129	Apr 27, 2020 (154)
139	Siberian	NC_000015.9 - 93815129	Apr 27, 2020 (154)
140	8.3KJPN	NC_000015.9 - 93815129	Apr 26, 2021 (155)
141	14KJPN	NC_000015.10 - 93271900	Oct 16, 2022 (156)
142	TopMed	NC_000015.10 - 93271900	Apr 26, 2021 (155)
143	UK 10K study - Twins	NC_000015.9 - 93815129	Oct 12, 2018 (152)
144	A Vietnamese Genetic Variation Database	NC_000015.9 - 93815129	Jul 13, 2019 (153)
145	ALFA	NC_000015.10 - 93271900	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)
rs58734713	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
175380, 211435, ss109048150, ss168511209, ss207327981, ss255211980, ss287004501, ss480259628, ss825422529, ss1397705280, ss1696127030, ss1713512686, ss3639064200, ss3639537783, ss3643086339, ss3847533543	NC_000015.8:91616132:T:C	NC_000015.10:93271899:T:C	(self)
67785233, 37645872, 159812, 26644192, 3977069, 16795853, 39987605, 14466542, 961319, 255999, 17541929, 35572130, 9459625, 75577234, 37645872, 8367545, ss236884962, ss480270471, ss481014780, ss484927721, ss536976347, ss660404423, ss778463276, ss782910179, ss783873395, ss832165112, ss833918996, ss992097001, ss1080351071, ss1354670718, ss1427720536, ss1577758196, ss1633643162, ss1676637195, ss1752178458, ss1935500007, ss1946402996, ss1959639565, ss1968177770, ss2028533942, ss2156943271, ss2628762014, ss2633269311, ss2701431282, ss2710823944, ss2938353075, ss2985692188, ss3013775526, ss3021663130, ss3351249688, ss3625681615, ss3627434410, ss3631259447, ss3633107799, ss3633812930, ss3634622132, ss3635501601, ss3636312699, ss3637252930, ss3638103459, ss3640329452, ss3641065414, ss3641360865, ss3644656110, ss3652066131, ss3680905944, ss3741181677, ss3744135629, ss3744922652, ss3753463458, ss3772421131, ss3834383633, ss3840794650, ss3883555150, ss3932810211, ss3984706471, ss3985735392, ss4017717684, ss5217607927, ss5237556418, ss5315808079, ss5421177894, ss5511524074, ss5624369189, ss5658108106, ss5799946755, ss5828611803, ss5847755348, ss5949533707, ss5979471646	NC_000015.9:93815128:T:C	NC_000015.10:93271899:T:C	(self)
88962497, 477866627, 1319147, 33146662, 1073416, 105679031, 217467919, 11143183339, ss2209219419, ss3028091185, ss3698488540, ss3725526640, ss3771851947, ss3818764962, ss3846284842, ss3976768661, ss5001922259, ss5299506262, ss5493112752, ss5601436562, ss5771841927, ss5815600670, ss5877091567	NC_000015.10:93271899:T:C	NC_000015.10:93271899:T:C	(self)
ss24668093, ss66217554, ss66772558, ss67189683, ss67569034, ss69185636, ss70667811, ss71229789, ss75750957, ss76364050, ss79092011, ss85394119, ss121802051, ss160449699, ss172859865, ss173388422	NT_010274.17:8780655:T:C	NC_000015.10:93271899:T:C	(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 rs17612678

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs17612678