Name: rs11730243
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.

rs11730243

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:105542556 (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: C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.451517 (119512/264690, TOPMED)
C=0.306120 (76334/249360, ALFA)
C=0.427529 (59731/139712, GnomAD) (+ 20 more)
T=0.43485 (34219/78692, PAGE_STUDY)
T=0.44858 (12676/28258, 14KJPN)
T=0.44385 (7439/16760, 8.3KJPN)
T=0.4839 (3099/6404, 1000G_30x)
T=0.4906 (2457/5008, 1000G)
C=0.2643 (1184/4480, Estonian)
C=0.2532 (976/3854, ALSPAC)
C=0.2635 (977/3708, TWINSUK)
T=0.3997 (1171/2930, KOREAN)
C=0.3949 (447/1132, Daghestan)
C=0.290 (289/998, GoNL)
T=0.356 (281/790, PRJEB37584)
C=0.285 (171/600, NorthernSweden)
C=0.325 (128/394, SGDP_PRJ)
T=0.479 (156/326, HapMap)
T=0.435 (94/216, Qatari)
T=0.316 (67/212, Vietnamese)
C=0.39 (18/46, Siberian)
C=0.38 (15/40, GENOME_DK)
C=0.12 (2/16, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC105377352 : Non Coding Transcript 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	249360	C=0.306120	T=0.693880	0.103401	0.491161	0.405438	32
European	Sub	219572	C=0.273960	T=0.726040	0.074791	0.52687	0.398339	0
African	Sub	9388	C=0.6737	T=0.3263	0.457605	0.110141	0.432254	1
African Others	Sub	342	C=0.787	T=0.213	0.608187	0.035088	0.356725	0
African American	Sub	9046	C=0.6695	T=0.3305	0.451912	0.112978	0.435109	1
Asian	Sub	3830	C=0.6245	T=0.3755	0.391123	0.142037	0.466841	0
East Asian	Sub	3100	C=0.6090	T=0.3910	0.372258	0.154194	0.473548	0
Other Asian	Sub	730	C=0.690	T=0.310	0.471233	0.090411	0.438356	0
Latin American 1	Sub	1026	C=0.4347	T=0.5653	0.183236	0.31384	0.502924	0
Latin American 2	Sub	6538	C=0.5116	T=0.4884	0.265525	0.242276	0.492199	0
South Asian	Sub	368	C=0.383	T=0.617	0.163043	0.396739	0.440217	1
Other	Sub	8638	C=0.4088	T=0.5912	0.183376	0.365825	0.450799	11

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	C=0.451517	T=0.548483
Allele Frequency Aggregator	Total	Global	249360	C=0.306120	T=0.693880
Allele Frequency Aggregator	European	Sub	219572	C=0.273960	T=0.726040
Allele Frequency Aggregator	African	Sub	9388	C=0.6737	T=0.3263
Allele Frequency Aggregator	Other	Sub	8638	C=0.4088	T=0.5912
Allele Frequency Aggregator	Latin American 2	Sub	6538	C=0.5116	T=0.4884
Allele Frequency Aggregator	Asian	Sub	3830	C=0.6245	T=0.3755
Allele Frequency Aggregator	Latin American 1	Sub	1026	C=0.4347	T=0.5653
Allele Frequency Aggregator	South Asian	Sub	368	C=0.383	T=0.617
gnomAD - Genomes	Global	Study-wide	139712	C=0.427529	T=0.572471
gnomAD - Genomes	European	Sub	75710	C=0.27838	T=0.72162
gnomAD - Genomes	African	Sub	41866	C=0.67236	T=0.32764
gnomAD - Genomes	American	Sub	13554	C=0.48170	T=0.51830
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.3708	T=0.6292
gnomAD - Genomes	East Asian	Sub	3118	C=0.5946	T=0.4054
gnomAD - Genomes	Other	Sub	2144	C=0.4160	T=0.5840
The PAGE Study	Global	Study-wide	78692	C=0.56515	T=0.43485
The PAGE Study	AfricanAmerican	Sub	32512	C=0.66415	T=0.33585
The PAGE Study	Mexican	Sub	10810	C=0.50342	T=0.49658
The PAGE Study	Asian	Sub	8318	C=0.5551	T=0.4449
The PAGE Study	PuertoRican	Sub	7918	C=0.4573	T=0.5427
The PAGE Study	NativeHawaiian	Sub	4534	C=0.4934	T=0.5066
The PAGE Study	Cuban	Sub	4226	C=0.3826	T=0.6174
The PAGE Study	Dominican	Sub	3828	C=0.5185	T=0.4815
The PAGE Study	CentralAmerican	Sub	2450	C=0.5743	T=0.4257
The PAGE Study	SouthAmerican	Sub	1980	C=0.5424	T=0.4576
The PAGE Study	NativeAmerican	Sub	1260	C=0.3952	T=0.6048
The PAGE Study	SouthAsian	Sub	856	C=0.446	T=0.554
14KJPN	JAPANESE	Study-wide	28258	C=0.55142	T=0.44858
8.3KJPN	JAPANESE	Study-wide	16760	C=0.55615	T=0.44385
1000Genomes_30x	Global	Study-wide	6404	C=0.5161	T=0.4839
1000Genomes_30x	African	Sub	1786	C=0.7531	T=0.2469
1000Genomes_30x	Europe	Sub	1266	C=0.2875	T=0.7125
1000Genomes_30x	South Asian	Sub	1202	C=0.3669	T=0.6331
1000Genomes_30x	East Asian	Sub	1170	C=0.5812	T=0.4188
1000Genomes_30x	American	Sub	980	C=0.485	T=0.515
1000Genomes	Global	Study-wide	5008	C=0.5094	T=0.4906
1000Genomes	African	Sub	1322	C=0.7443	T=0.2557
1000Genomes	East Asian	Sub	1008	C=0.5873	T=0.4127
1000Genomes	Europe	Sub	1006	C=0.2893	T=0.7107
1000Genomes	South Asian	Sub	978	C=0.359	T=0.641
1000Genomes	American	Sub	694	C=0.480	T=0.520
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.2643	T=0.7357
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.2532	T=0.7468
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.2635	T=0.7365
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.6003	T=0.3997
Genome-wide autozygosity in Daghestan	Global	Study-wide	1132	C=0.3949	T=0.6051
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.408	T=0.592
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.431	T=0.569
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.451	T=0.549
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.296	T=0.704
Genome-wide autozygosity in Daghestan	South Asian	Sub	94	C=0.31	T=0.69
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.36	T=0.64
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.290	T=0.710
CNV burdens in cranial meningiomas	Global	Study-wide	790	C=0.644	T=0.356
CNV burdens in cranial meningiomas	CRM	Sub	790	C=0.644	T=0.356
Northern Sweden	ACPOP	Study-wide	600	C=0.285	T=0.715
SGDP_PRJ	Global	Study-wide	394	C=0.325	T=0.675
HapMap	Global	Study-wide	326	C=0.521	T=0.479
HapMap	American	Sub	120	C=0.317	T=0.683
HapMap	African	Sub	118	C=0.737	T=0.263
HapMap	Asian	Sub	88	C=0.51	T=0.49
Qatari	Global	Study-wide	216	C=0.565	T=0.435
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.684	T=0.316
Siberian	Global	Study-wide	46	C=0.39	T=0.61
The Danish reference pan genome	Danish	Study-wide	40	C=0.38	T=0.62
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	16	C=0.12	T=0.88

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 4	NC_000004.12:g.105542556C>T
GRCh37.p13 chr 4	NC_000004.11:g.106463713C>T

Gene: LOC105377352, uncharacterized LOC105377352 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105377352 transcript variant X5	XR_001741411.1:n.940G>A	N/A	Non Coding Transcript Variant
LOC105377352 transcript variant X1	XR_939038.3:n.556G>A	N/A	Non Coding Transcript Variant
LOC105377352 transcript variant X4	XR_001741410.2:n.557G>A	N/A	Non Coding Transcript Variant
LOC105377352 transcript variant X6	XR_001741413.2:n.561G>A	N/A	Non Coding Transcript Variant
LOC105377352 transcript variant X2	XR_001741412.2:n.	N/A	Intron Variant
LOC105377352 transcript variant X7	XR_001741414.2:n.	N/A	Intron Variant
LOC105377352 transcript variant X3	XR_939040.3: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	C=	T
GRCh38.p14 chr 4	NC_000004.12:g.105542556=	NC_000004.12:g.105542556C>T
GRCh37.p13 chr 4	NC_000004.11:g.106463713=	NC_000004.11:g.106463713C>T
LOC105377352 transcript variant X1	XR_939038.3:n.556=	XR_939038.3:n.556G>A
LOC105377352 transcript variant X2	XR_939038.2:n.464=	XR_939038.2:n.464G>A
LOC105377352 transcript variant X1	XR_939038.1:n.449=	XR_939038.1:n.449G>A
LOC105377352 transcript variant X4	XR_001741410.2:n.557=	XR_001741410.2:n.557G>A
LOC105377352 transcript variant X1	XR_001741410.1:n.464=	XR_001741410.1:n.464G>A
LOC105377352 transcript variant X6	XR_001741413.2:n.561=	XR_001741413.2:n.561G>A
LOC105377352 transcript variant X5	XR_001741413.1:n.464=	XR_001741413.1:n.464G>A
LOC105377352 transcript variant X5	XR_001741411.1:n.940=	XR_001741411.1:n.940G>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#.

119 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	CSHL-HAPMAP	ss17022405	Feb 28, 2004 (120)
2	SSAHASNP	ss22050839	Apr 05, 2004 (121)
3	PERLEGEN	ss24169546	Sep 20, 2004 (123)
4	ABI	ss44575599	Mar 13, 2006 (126)
5	HGSV	ss77414037	Dec 07, 2007 (129)
6	BCMHGSC_JDW	ss92717082	Mar 24, 2008 (129)
7	HUMANGENOME_JCVI	ss98990053	Feb 05, 2009 (130)
8	1000GENOMES	ss108201251	Jan 23, 2009 (130)
9	1000GENOMES	ss110352639	Jan 24, 2009 (130)
10	ENSEMBL	ss133263543	Dec 01, 2009 (131)
11	ENSEMBL	ss139801465	Dec 01, 2009 (131)
12	GMI	ss157698278	Dec 01, 2009 (131)
13	ILLUMINA	ss159998435	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss162412177	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss163996157	Jul 04, 2010 (132)
16	BUSHMAN	ss198973322	Jul 04, 2010 (132)
17	BCM-HGSC-SUB	ss206363849	Jul 04, 2010 (132)
18	1000GENOMES	ss221121931	Jul 14, 2010 (132)
19	1000GENOMES	ss232531188	Jul 14, 2010 (132)
20	1000GENOMES	ss239792050	Jul 15, 2010 (132)
21	BL	ss253399757	May 09, 2011 (134)
22	GMI	ss277860191	May 04, 2012 (137)
23	GMI	ss284975320	Apr 25, 2013 (138)
24	PJP	ss293155412	May 09, 2011 (134)
25	ILLUMINA	ss479577800	May 04, 2012 (137)
26	ILLUMINA	ss479582049	May 04, 2012 (137)
27	ILLUMINA	ss480059500	Sep 08, 2015 (146)
28	ILLUMINA	ss484587644	May 04, 2012 (137)
29	ILLUMINA	ss536717434	Sep 08, 2015 (146)
30	TISHKOFF	ss557748143	Apr 25, 2013 (138)
31	SSMP	ss651550666	Apr 25, 2013 (138)
32	ILLUMINA	ss778389445	Sep 08, 2015 (146)
33	ILLUMINA	ss782740608	Sep 08, 2015 (146)
34	ILLUMINA	ss783707579	Sep 08, 2015 (146)
35	ILLUMINA	ss831992522	Sep 08, 2015 (146)
36	ILLUMINA	ss833844502	Sep 08, 2015 (146)
37	EVA-GONL	ss980497903	Aug 21, 2014 (142)
38	JMKIDD_LAB	ss1071820615	Aug 21, 2014 (142)
39	1000GENOMES	ss1311150633	Aug 21, 2014 (142)
40	HAMMER_LAB	ss1397384575	Sep 08, 2015 (146)
41	DDI	ss1429996221	Apr 01, 2015 (144)
42	EVA_GENOME_DK	ss1580704403	Apr 01, 2015 (144)
43	EVA_DECODE	ss1590002311	Apr 01, 2015 (144)
44	EVA_UK10K_ALSPAC	ss1610829848	Apr 01, 2015 (144)
45	EVA_UK10K_TWINSUK	ss1653823881	Apr 01, 2015 (144)
46	ILLUMINA	ss1752490944	Sep 08, 2015 (146)
47	WEILL_CORNELL_DGM	ss1923736106	Feb 12, 2016 (147)
48	ILLUMINA	ss1946123916	Feb 12, 2016 (147)
49	ILLUMINA	ss1958710021	Feb 12, 2016 (147)
50	GENOMED	ss1969826665	Jul 19, 2016 (147)
51	JJLAB	ss2022452873	Sep 14, 2016 (149)
52	USC_VALOUEV	ss2150582446	Dec 20, 2016 (150)
53	HUMAN_LONGEVITY	ss2265780738	Dec 20, 2016 (150)
54	SYSTEMSBIOZJU	ss2625724281	Nov 08, 2017 (151)
55	ILLUMINA	ss2634159444	Nov 08, 2017 (151)
56	ILLUMINA	ss2634159445	Nov 08, 2017 (151)
57	ILLUMINA	ss2635135747	Nov 08, 2017 (151)
58	GRF	ss2706060211	Nov 08, 2017 (151)
59	ILLUMINA	ss2711012939	Nov 08, 2017 (151)
60	GNOMAD	ss2813349210	Nov 08, 2017 (151)
61	AFFY	ss2985299732	Nov 08, 2017 (151)
62	AFFY	ss2985927971	Nov 08, 2017 (151)
63	SWEGEN	ss2995280793	Nov 08, 2017 (151)
64	ILLUMINA	ss3022402136	Nov 08, 2017 (151)
65	BIOINF_KMB_FNS_UNIBA	ss3025001885	Nov 08, 2017 (151)
66	CSHL	ss3345881549	Nov 08, 2017 (151)
67	ILLUMINA	ss3625850935	Oct 12, 2018 (152)
68	ILLUMINA	ss3629033994	Oct 12, 2018 (152)
69	ILLUMINA	ss3632093531	Oct 12, 2018 (152)
70	ILLUMINA	ss3633344487	Oct 12, 2018 (152)
71	ILLUMINA	ss3634063832	Oct 12, 2018 (152)
72	ILLUMINA	ss3634964949	Oct 12, 2018 (152)
73	ILLUMINA	ss3635746535	Oct 12, 2018 (152)
74	ILLUMINA	ss3636669413	Oct 12, 2018 (152)
75	ILLUMINA	ss3637499078	Oct 12, 2018 (152)
76	ILLUMINA	ss3640672242	Oct 12, 2018 (152)
77	ILLUMINA	ss3644856724	Oct 12, 2018 (152)
78	URBANLAB	ss3647811501	Oct 12, 2018 (152)
79	ILLUMINA	ss3652889557	Oct 12, 2018 (152)
80	ILLUMINA	ss3654071689	Oct 12, 2018 (152)
81	EGCUT_WGS	ss3663179045	Jul 13, 2019 (153)
82	EVA_DECODE	ss3712740877	Jul 13, 2019 (153)
83	ILLUMINA	ss3726158919	Jul 13, 2019 (153)
84	ACPOP	ss3731459734	Jul 13, 2019 (153)
85	ILLUMINA	ss3744239192	Jul 13, 2019 (153)
86	ILLUMINA	ss3745265213	Jul 13, 2019 (153)
87	EVA	ss3762215448	Jul 13, 2019 (153)
88	PAGE_CC	ss3771144982	Jul 13, 2019 (153)
89	ILLUMINA	ss3772759725	Jul 13, 2019 (153)
90	PACBIO	ss3784812193	Jul 13, 2019 (153)
91	PACBIO	ss3790255153	Jul 13, 2019 (153)
92	PACBIO	ss3795130502	Jul 13, 2019 (153)
93	KHV_HUMAN_GENOMES	ss3805365140	Jul 13, 2019 (153)
94	EVA	ss3828724321	Apr 26, 2020 (154)
95	EVA	ss3837804112	Apr 26, 2020 (154)
96	EVA	ss3843242723	Apr 26, 2020 (154)
97	SGDP_PRJ	ss3859699098	Apr 26, 2020 (154)
98	KRGDB	ss3905982442	Apr 26, 2020 (154)
99	EVA	ss3984532822	Apr 26, 2021 (155)
100	EVA	ss3985087452	Apr 26, 2021 (155)
101	EVA	ss4017161446	Apr 26, 2021 (155)
102	TOPMED	ss4626168513	Apr 26, 2021 (155)
103	TOMMO_GENOMICS	ss5167265508	Apr 26, 2021 (155)
104	1000G_HIGH_COVERAGE	ss5260437070	Oct 13, 2022 (156)
105	EVA	ss5314980240	Oct 13, 2022 (156)
106	EVA	ss5351244640	Oct 13, 2022 (156)
107	HUGCELL_USP	ss5459062609	Oct 13, 2022 (156)
108	EVA	ss5507659682	Oct 13, 2022 (156)
109	1000G_HIGH_COVERAGE	ss5542182958	Oct 13, 2022 (156)
110	SANFORD_IMAGENETICS	ss5624563706	Oct 13, 2022 (156)
111	SANFORD_IMAGENETICS	ss5635751529	Oct 13, 2022 (156)
112	TOMMO_GENOMICS	ss5702049803	Oct 13, 2022 (156)
113	EVA	ss5799623211	Oct 13, 2022 (156)
114	YY_MCH	ss5805389181	Oct 13, 2022 (156)
115	EVA	ss5844481978	Oct 13, 2022 (156)
116	EVA	ss5848020462	Oct 13, 2022 (156)
117	EVA	ss5854372680	Oct 13, 2022 (156)
118	EVA	ss5864847055	Oct 13, 2022 (156)
119	EVA	ss5964147415	Oct 13, 2022 (156)
120	1000Genomes	NC_000004.11 - 106463713	Oct 12, 2018 (152)
121	1000Genomes_30x	NC_000004.12 - 105542556	Oct 13, 2022 (156)
122	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 106463713	Oct 12, 2018 (152)
123	Genome-wide autozygosity in Daghestan	NC_000004.10 - 106683162	Apr 26, 2020 (154)
124	Genetic variation in the Estonian population	NC_000004.11 - 106463713	Oct 12, 2018 (152)
125	The Danish reference pan genome	NC_000004.11 - 106463713	Apr 26, 2020 (154)
126	gnomAD - Genomes	NC_000004.12 - 105542556	Apr 26, 2021 (155)
127	Genome of the Netherlands Release 5	NC_000004.11 - 106463713	Apr 26, 2020 (154)
128	HapMap	NC_000004.12 - 105542556	Apr 26, 2020 (154)
129	KOREAN population from KRGDB	NC_000004.11 - 106463713	Apr 26, 2020 (154)
130	Northern Sweden	NC_000004.11 - 106463713	Jul 13, 2019 (153)
131	The PAGE Study	NC_000004.12 - 105542556	Jul 13, 2019 (153)
132	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 106463713	Apr 26, 2021 (155)
133	CNV burdens in cranial meningiomas	NC_000004.11 - 106463713	Apr 26, 2021 (155)
134	Qatari	NC_000004.11 - 106463713	Apr 26, 2020 (154)
135	SGDP_PRJ	NC_000004.11 - 106463713	Apr 26, 2020 (154)
136	Siberian	NC_000004.11 - 106463713	Apr 26, 2020 (154)
137	8.3KJPN	NC_000004.11 - 106463713	Apr 26, 2021 (155)
138	14KJPN	NC_000004.12 - 105542556	Oct 13, 2022 (156)
139	TopMed	NC_000004.12 - 105542556	Apr 26, 2021 (155)
140	UK 10K study - Twins	NC_000004.11 - 106463713	Oct 12, 2018 (152)
141	A Vietnamese Genetic Variation Database	NC_000004.11 - 106463713	Jul 13, 2019 (153)
142	ALFA	NC_000004.12 - 105542556	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)
rs17584256	Oct 07, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77414037	NC_000004.9:106821316:C:T	NC_000004.12:105542555:C:T	(self)
359962, ss92717082, ss108201251, ss110352639, ss162412177, ss163996157, ss198973322, ss206363849, ss253399757, ss277860191, ss284975320, ss293155412, ss479577800, ss1397384575, ss1590002311, ss2635135747	NC_000004.10:106683161:C:T	NC_000004.12:105542555:C:T	(self)
22599371, 12574893, 8917293, 6869342, 5560354, 13159836, 4744599, 313379, 82183, 5778036, 11716078, 3098800, 25234815, 12574893, 2764504, ss221121931, ss232531188, ss239792050, ss479582049, ss480059500, ss484587644, ss536717434, ss557748143, ss651550666, ss778389445, ss782740608, ss783707579, ss831992522, ss833844502, ss980497903, ss1071820615, ss1311150633, ss1429996221, ss1580704403, ss1610829848, ss1653823881, ss1752490944, ss1923736106, ss1946123916, ss1958710021, ss1969826665, ss2022452873, ss2150582446, ss2625724281, ss2634159444, ss2634159445, ss2706060211, ss2711012939, ss2813349210, ss2985299732, ss2985927971, ss2995280793, ss3022402136, ss3345881549, ss3625850935, ss3629033994, ss3632093531, ss3633344487, ss3634063832, ss3634964949, ss3635746535, ss3636669413, ss3637499078, ss3640672242, ss3644856724, ss3652889557, ss3654071689, ss3663179045, ss3731459734, ss3744239192, ss3745265213, ss3762215448, ss3772759725, ss3784812193, ss3790255153, ss3795130502, ss3828724321, ss3837804112, ss3859699098, ss3905982442, ss3984532822, ss3985087452, ss4017161446, ss5167265508, ss5314980240, ss5351244640, ss5507659682, ss5624563706, ss5635751529, ss5799623211, ss5844481978, ss5848020462, ss5964147415	NC_000004.11:106463712:C:T	NC_000004.12:105542555:C:T	(self)
29708893, 160103856, 2677888, 366451, 35886907, 463546069, 14965259522, ss2265780738, ss3025001885, ss3647811501, ss3712740877, ss3726158919, ss3771144982, ss3805365140, ss3843242723, ss4626168513, ss5260437070, ss5459062609, ss5542182958, ss5702049803, ss5805389181, ss5854372680, ss5864847055	NC_000004.12:105542555:C:T	NC_000004.12:105542555:C:T	(self)
ss17022405, ss22050839	NT_016354.16:30958842:C:T	NC_000004.12:105542555:C:T	(self)
ss24169546, ss44575599, ss98990053, ss133263543, ss139801465, ss157698278, ss159998435	NT_016354.19:31011433:C:T	NC_000004.12:105542555:C: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 rs11730243

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

rs11730243