Name: rs35356968
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.

rs35356968

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:36816602-36816618 (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: del(A)₁₀ / del(A)₇ / del(A)₅ / del…
del(A)₁₀ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dup(A)₇ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₇=0.2939 (1472/5008, 1000G)
delAA=0.1258 (485/3854, ALSPAC)
del(A)₁₀=0.000 (0/122, ALFA) (+ 6 more)
del(A)₇=0.000 (0/122, ALFA)
del(A)₄=0.000 (0/122, ALFA)
delAAA=0.000 (0/122, ALFA)
delAA=0.000 (0/122, ALFA)
delA=0.000 (0/122, ALFA)
dupA=0.000 (0/122, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC124903158 : 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	122	AAAAAAAAAAAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	16	AAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	90	AAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	90	AAAAAAAAAAAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAA=1.0	AAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAA=1.0	AAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	2	AAAAAAAAAAAAAAAAA=1.0	AAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	10	AAAAAAAAAAAAAAAAA=1.0	AAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A

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
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.2939	delA=0.7061
1000Genomes	African	Sub	1322	(A)₁₇=0.4047	delA=0.5953
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.2778	delA=0.7222
1000Genomes	Europe	Sub	1006	(A)₁₇=0.2058	delA=0.7942
1000Genomes	South Asian	Sub	978	(A)₁₇=0.327	delA=0.673
1000Genomes	American	Sub	694	(A)₁₇=0.187	delA=0.813
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₇=0.8742	delAA=0.1258
Allele Frequency Aggregator	Total	Global	122	(A)₁₇=1.000	del(A)₁₀=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	African	Sub	90	(A)₁₇=1.00	del(A)₁₀=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	European	Sub	16	(A)₁₇=1.00	del(A)₁₀=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Other	Sub	10	(A)₁₇=1.0	del(A)₁₀=0.0, del(A)₇=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₁₇=1.0	del(A)₁₀=0.0, del(A)₇=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(A)₁₇=1.0	del(A)₁₀=0.0, del(A)₇=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₇=0	del(A)₁₀=0, del(A)₇=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₇=0	del(A)₁₀=0, del(A)₇=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0

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 13	NC_000013.11:g.36816609_36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816612_36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816614_36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816615_36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816616_36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816617_36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816618del
GRCh38.p14 chr 13	NC_000013.11:g.36816618dup
GRCh38.p14 chr 13	NC_000013.11:g.36816612_36816618dup
GRCh38.p14 chr 13	NC_000013.11:g.36816611_36816618dup
GRCh37.p13 chr 13	NC_000013.10:g.37390746_37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390749_37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390751_37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390752_37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390753_37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390754_37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390755del
GRCh37.p13 chr 13	NC_000013.10:g.37390755dup
GRCh37.p13 chr 13	NC_000013.10:g.37390749_37390755dup
GRCh37.p13 chr 13	NC_000013.10:g.37390748_37390755dup
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2408_2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2411_2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2413_2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2414_2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2415_2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2416_2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2417del
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2417dup
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2411_2417dup
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2410_2417dup

Gene: LOC124903158, uncharacterized LOC124903158 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124903158 transcript	XR_007063760.1: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	(A)₁₇=	del(A)₁₀	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dup(A)₇	dup(A)₈
GRCh38.p14 chr 13	NC_000013.11:g.36816602_36816618=	NC_000013.11:g.36816609_36816618del	NC_000013.11:g.36816612_36816618del	NC_000013.11:g.36816614_36816618del	NC_000013.11:g.36816615_36816618del	NC_000013.11:g.36816616_36816618del	NC_000013.11:g.36816617_36816618del	NC_000013.11:g.36816618del	NC_000013.11:g.36816618dup	NC_000013.11:g.36816612_36816618dup	NC_000013.11:g.36816611_36816618dup
GRCh37.p13 chr 13	NC_000013.10:g.37390739_37390755=	NC_000013.10:g.37390746_37390755del	NC_000013.10:g.37390749_37390755del	NC_000013.10:g.37390751_37390755del	NC_000013.10:g.37390752_37390755del	NC_000013.10:g.37390753_37390755del	NC_000013.10:g.37390754_37390755del	NC_000013.10:g.37390755del	NC_000013.10:g.37390755dup	NC_000013.10:g.37390749_37390755dup	NC_000013.10:g.37390748_37390755dup
RFXAP RefSeqGene (LRG_103)	NG_007876.1:g.2401_2417=	NG_007876.1:g.2408_2417del	NG_007876.1:g.2411_2417del	NG_007876.1:g.2413_2417del	NG_007876.1:g.2414_2417del	NG_007876.1:g.2415_2417del	NG_007876.1:g.2416_2417del	NG_007876.1:g.2417del	NG_007876.1:g.2417dup	NG_007876.1:g.2411_2417dup	NG_007876.1:g.2410_2417dup

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#.

57 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40308946	Mar 14, 2006 (126)
2	HGSV	ss78013008	Dec 07, 2007 (129)
3	HGSV	ss80945199	Dec 15, 2007 (130)
4	HUMANGENOME_JCVI	ss95763724	Feb 05, 2009 (130)
5	BCMHGSC_JDW	ss103544873	Mar 15, 2016 (147)
6	PJP	ss294792238	May 09, 2011 (134)
7	PJP	ss294792239	May 09, 2011 (137)
8	SSMP	ss664173646	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666595434	Apr 25, 2013 (138)
10	SSIP	ss947312599	Aug 21, 2014 (142)
11	1000GENOMES	ss1373039813	Aug 21, 2014 (142)
12	EVA_UK10K_ALSPAC	ss1707748081	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1707748093	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1710597283	Apr 01, 2015 (144)
15	EVA_UK10K_ALSPAC	ss1710597284	Apr 01, 2015 (144)
16	SWEGEN	ss3010868279	Nov 08, 2017 (151)
17	MCHAISSO	ss3063760739	Nov 08, 2017 (151)
18	MCHAISSO	ss3064591721	Nov 08, 2017 (151)
19	MCHAISSO	ss3065515448	Nov 08, 2017 (151)
20	EVA_DECODE	ss3695107089	Jul 13, 2019 (153)
21	EVA_DECODE	ss3695107090	Jul 13, 2019 (153)
22	EVA_DECODE	ss3695107091	Jul 13, 2019 (153)
23	EVA_DECODE	ss3695107092	Jul 13, 2019 (153)
24	EVA_DECODE	ss3695107093	Jul 13, 2019 (153)
25	PACBIO	ss3787430805	Jul 13, 2019 (153)
26	PACBIO	ss3792501132	Jul 13, 2019 (153)
27	PACBIO	ss3797384894	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3816679195	Jul 13, 2019 (153)
29	EVA	ss3833497537	Apr 27, 2020 (154)
30	GNOMAD	ss4264252900	Apr 26, 2021 (155)
31	GNOMAD	ss4264252901	Apr 26, 2021 (155)
32	GNOMAD	ss4264252902	Apr 26, 2021 (155)
33	GNOMAD	ss4264252903	Apr 26, 2021 (155)
34	GNOMAD	ss4264252904	Apr 26, 2021 (155)
35	GNOMAD	ss4264252905	Apr 26, 2021 (155)
36	GNOMAD	ss4264252906	Apr 26, 2021 (155)
37	GNOMAD	ss4264252907	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5209576748	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5209576749	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5209576750	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5209576751	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5293409913	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5293409914	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5293409915	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5293409916	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5487806740	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5487806741	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5487806742	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5761332474	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5761332475	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5761332476	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5761332477	Oct 16, 2022 (156)
53	EVA	ss5839347056	Oct 16, 2022 (156)
54	EVA	ss5839347057	Oct 16, 2022 (156)
55	EVA	ss5839347058	Oct 16, 2022 (156)
56	EVA	ss5850687156	Oct 16, 2022 (156)
57	EVA	ss5980786391	Oct 16, 2022 (156)
58	1000Genomes	NC_000013.10 - 37390739	Oct 12, 2018 (152)
59	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 37390739	Oct 12, 2018 (152)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 428058506 (NC_000013.11:36816601::A 242/98952) Row 428058507 (NC_000013.11:36816601::AAAAAAAA 2/98958) Row 428058508 (NC_000013.11:36816601:A: 83375/98958)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 67546055 (NC_000013.10:37390738:A: 13208/16718) Row 67546056 (NC_000013.10:37390738:AA: 39/16718) Row 67546057 (NC_000013.10:37390738::A 3/16718)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 67546055 (NC_000013.10:37390738:A: 13208/16718) Row 67546056 (NC_000013.10:37390738:AA: 39/16718) Row 67546057 (NC_000013.10:37390738::A 3/16718)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 67546055 (NC_000013.10:37390738:A: 13208/16718) Row 67546056 (NC_000013.10:37390738:AA: 39/16718) Row 67546057 (NC_000013.10:37390738::A 3/16718)...	-	Apr 26, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 67546055 (NC_000013.10:37390738:A: 13208/16718) Row 67546056 (NC_000013.10:37390738:AA: 39/16718) Row 67546057 (NC_000013.10:37390738::A 3/16718)...	-	Apr 26, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 95169578 (NC_000013.11:36816601:A: 22841/28244) Row 95169579 (NC_000013.11:36816601::A 3/28244) Row 95169580 (NC_000013.11:36816601:AA: 59/28244)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 95169578 (NC_000013.11:36816601:A: 22841/28244) Row 95169579 (NC_000013.11:36816601::A 3/28244) Row 95169580 (NC_000013.11:36816601:AA: 59/28244)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 95169578 (NC_000013.11:36816601:A: 22841/28244) Row 95169579 (NC_000013.11:36816601::A 3/28244) Row 95169580 (NC_000013.11:36816601:AA: 59/28244)...	-	Oct 16, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 95169578 (NC_000013.11:36816601:A: 22841/28244) Row 95169579 (NC_000013.11:36816601::A 3/28244) Row 95169580 (NC_000013.11:36816601:AA: 59/28244)...	-	Oct 16, 2022 (156)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33723776 (NC_000013.10:37390739:A: 3265/3708) Row 33723777 (NC_000013.10:37390738:AA: 434/3708)	-	Apr 27, 2020 (154)
77	UK 10K study - Twins	-	Oct 12, 2018 (152)
78	ALFA	NC_000013.11 - 36816602	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)
rs369416916	May 13, 2013 (138)
rs58453216	May 24, 2008 (130)
rs79161385	Oct 26, 2010 (133)
rs139974971	May 04, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAA	(self)
ss5209576751	NC_000013.10:37390738:AAAAAAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4264252907, ss5293409914, ss5487806742, ss5761332477	NC_000013.11:36816601:AAAAAAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4264252906	NC_000013.11:36816601:AAAAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3695107093, ss4264252905	NC_000013.11:36816601:AAAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss103544873	NT_024524.14:18370751:AAAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4264252904	NC_000013.11:36816601:AAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3695107092	NC_000013.11:36816602:AAA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
33723777, ss1707748081, ss1707748093, ss3010868279, ss5209576749, ss5839347057	NC_000013.10:37390738:AA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4264252903, ss5293409915, ss5487806741, ss5761332476	NC_000013.11:36816601:AA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3695107091	NC_000013.11:36816603:AA:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss294792238	NC_000013.9:36288738:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss78013008, ss80945199, ss294792239	NC_000013.9:36288754:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
60709703, ss664173646, ss666595434, ss1373039813, ss3787430805, ss3792501132, ss3797384894, ss3833497537, ss5209576748, ss5839347056, ss5980786391	NC_000013.10:37390738:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss947312599, ss1710597283, ss1710597284	NC_000013.10:37390739:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3063760739, ss3064591721, ss3065515448, ss3816679195, ss4264252902, ss5293409913, ss5487806740, ss5761332474, ss5850687156	NC_000013.11:36816601:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3695107090	NC_000013.11:36816604:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40308946	NT_024524.14:18370738:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss95763724	NT_024524.14:18370754:A:	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5209576750	NC_000013.10:37390738::A	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4264252900, ss5293409916, ss5761332475	NC_000013.11:36816601::A	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
1030352888	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5839347058	NC_000013.10:37390738::AAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
ss4264252901	NC_000013.11:36816601::AAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3695107089	NC_000013.11:36816605::AAAAAAAA	NC_000013.11:36816601:AAAAAAAAAAAA… NC_000013.11:36816601:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35356968

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

rs35356968