Name: rs34262146
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.

rs34262146

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:35510834-35510846 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.0209 (138/6598, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLFN12L : 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	6598	AAAAAAAAAAAAA=0.9791	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0209, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	0.960594	0.002425	0.036981	17
European	Sub	5276	AAAAAAAAAAAAA=0.9795	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0205, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	0.960197	0.001137	0.038666	2
African	Sub	730	AAAAAAAAAAAAA=0.964	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.036, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	0.939726	0.010959	0.049315	16
African Others	Sub	28	AAAAAAAAAAAAA=0.93	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.07, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	0.857143	0.0	0.142857	0
African American	Sub	702	AAAAAAAAAAAAA=0.966	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.034, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	0.94302	0.011396	0.045584	18
Asian	Sub	48	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	36	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	56	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	296	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	172	AAAAAAAAAAAAA=0.977	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.023, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	0.965116	0.011628	0.023256	12

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
Allele Frequency Aggregator	Total	Global	6598	(A)₁₃=0.9791	delAA=0.0000, delA=0.0000, dupA=0.0209, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	5276	(A)₁₃=0.9795	delAA=0.0000, delA=0.0000, dupA=0.0205, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	730	(A)₁₃=0.964	delAA=0.000, delA=0.000, dupA=0.036, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	296	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	172	(A)₁₃=0.977	delAA=0.000, delA=0.000, dupA=0.023, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	56	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	48	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00

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 17	NC_000017.11:g.35510844_35510846del
GRCh38.p14 chr 17	NC_000017.11:g.35510845_35510846del
GRCh38.p14 chr 17	NC_000017.11:g.35510846del
GRCh38.p14 chr 17	NC_000017.11:g.35510846dup
GRCh38.p14 chr 17	NC_000017.11:g.35510845_35510846dup
GRCh38.p14 chr 17	NC_000017.11:g.35510844_35510846dup
GRCh38.p14 chr 17	NC_000017.11:g.35510843_35510846dup
GRCh38.p14 chr 17	NC_000017.11:g.35510842_35510846dup
GRCh37.p13 chr 17	NC_000017.10:g.33837863_33837865del
GRCh37.p13 chr 17	NC_000017.10:g.33837864_33837865del
GRCh37.p13 chr 17	NC_000017.10:g.33837865del
GRCh37.p13 chr 17	NC_000017.10:g.33837865dup
GRCh37.p13 chr 17	NC_000017.10:g.33837864_33837865dup
GRCh37.p13 chr 17	NC_000017.10:g.33837863_33837865dup
GRCh37.p13 chr 17	NC_000017.10:g.33837862_33837865dup
GRCh37.p13 chr 17	NC_000017.10:g.33837861_33837865dup

Gene: SLFN12L, schlafen family member 12 like (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLFN12L transcript variant 2	NM_001195790.3:c.-288+114… NM_001195790.3:c.-288+11443_-288+11445del	N/A	Intron Variant
SLFN12L transcript variant 1	NM_001363830.2:c.86+11443… NM_001363830.2:c.86+11443_86+11445del	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)₁₃=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 17	NC_000017.11:g.35510834_35510846=	NC_000017.11:g.35510844_35510846del	NC_000017.11:g.35510845_35510846del	NC_000017.11:g.35510846del	NC_000017.11:g.35510846dup	NC_000017.11:g.35510845_35510846dup	NC_000017.11:g.35510844_35510846dup	NC_000017.11:g.35510843_35510846dup	NC_000017.11:g.35510842_35510846dup
GRCh37.p13 chr 17	NC_000017.10:g.33837853_33837865=	NC_000017.10:g.33837863_33837865del	NC_000017.10:g.33837864_33837865del	NC_000017.10:g.33837865del	NC_000017.10:g.33837865dup	NC_000017.10:g.33837864_33837865dup	NC_000017.10:g.33837863_33837865dup	NC_000017.10:g.33837862_33837865dup	NC_000017.10:g.33837861_33837865dup
SLFN12L transcript variant 2	NM_001195790.3:c.-288+11445=	NM_001195790.3:c.-288+11443_-288+11445del	NM_001195790.3:c.-288+11444_-288+11445del	NM_001195790.3:c.-288+11445del	NM_001195790.3:c.-288+11445dup	NM_001195790.3:c.-288+11444_-288+11445dup	NM_001195790.3:c.-288+11443_-288+11445dup	NM_001195790.3:c.-288+11442_-288+11445dup	NM_001195790.3:c.-288+11441_-288+11445dup
SLFN12L transcript variant 1	NM_001363830.2:c.86+11445=	NM_001363830.2:c.86+11443_86+11445del	NM_001363830.2:c.86+11444_86+11445del	NM_001363830.2:c.86+11445del	NM_001363830.2:c.86+11445dup	NM_001363830.2:c.86+11444_86+11445dup	NM_001363830.2:c.86+11443_86+11445dup	NM_001363830.2:c.86+11442_86+11445dup	NM_001363830.2:c.86+11441_86+11445dup

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#.

60 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40804724	Mar 13, 2006 (126)
2	HGSV	ss79866882	Dec 15, 2007 (130)
3	HGSV	ss79931080	Dec 15, 2007 (130)
4	PJP	ss294910885	May 09, 2011 (134)
5	SSMP	ss664353390	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666689736	Apr 25, 2013 (138)
7	EVA_UK10K_ALSPAC	ss1708740353	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1708740355	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1708740437	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1708740438	Apr 01, 2015 (144)
11	SWEGEN	ss3015455632	Nov 08, 2017 (151)
12	EVA_DECODE	ss3700375959	Jul 13, 2019 (153)
13	EVA_DECODE	ss3700375960	Jul 13, 2019 (153)
14	EVA_DECODE	ss3700375961	Jul 13, 2019 (153)
15	EVA_DECODE	ss3700375962	Jul 13, 2019 (153)
16	EVA_DECODE	ss3700375963	Jul 13, 2019 (153)
17	EVA_DECODE	ss3700375964	Jul 13, 2019 (153)
18	ACPOP	ss3741989590	Jul 13, 2019 (153)
19	ACPOP	ss3741989591	Jul 13, 2019 (153)
20	ACPOP	ss3741989592	Jul 13, 2019 (153)
21	PACBIO	ss3793150823	Jul 13, 2019 (153)
22	PACBIO	ss3798036746	Jul 13, 2019 (153)
23	EVA	ss3834845936	Apr 27, 2020 (154)
24	EVA	ss3841033187	Apr 27, 2020 (154)
25	EVA	ss3846530238	Apr 27, 2020 (154)
26	KOGIC	ss3978782891	Apr 27, 2020 (154)
27	KOGIC	ss3978782892	Apr 27, 2020 (154)
28	KOGIC	ss3978782893	Apr 27, 2020 (154)
29	KOGIC	ss3978782894	Apr 27, 2020 (154)
30	KOGIC	ss3978782895	Apr 27, 2020 (154)
31	GNOMAD	ss4310734666	Apr 26, 2021 (155)
32	GNOMAD	ss4310734667	Apr 26, 2021 (155)
33	GNOMAD	ss4310734668	Apr 26, 2021 (155)
34	GNOMAD	ss4310734669	Apr 26, 2021 (155)
35	GNOMAD	ss4310734670	Apr 26, 2021 (155)
36	GNOMAD	ss4310734671	Apr 26, 2021 (155)
37	GNOMAD	ss4310734672	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5222186762	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5222186763	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5222186764	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5222186765	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5222186766	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5222186767	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5302968889	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5302968890	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5302968891	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5302968892	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5302968893	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5302968894	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5496049239	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5496049240	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5496049241	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5496049242	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5778320847	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5778320848	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5778320849	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5778320850	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5778320851	Oct 16, 2022 (156)
59	EVA	ss5833920850	Oct 16, 2022 (156)
60	EVA	ss5833920851	Oct 16, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39750910 (NC_000017.10:33837852::AAA 477/3854) Row 39750911 (NC_000017.10:33837852::AA 779/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39750910 (NC_000017.10:33837852::AAA 477/3854) Row 39750911 (NC_000017.10:33837852::AA 779/3854)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 505879471 (NC_000017.11:35510833::A 20836/127948) Row 505879472 (NC_000017.11:35510833::AA 17319/127986) Row 505879473 (NC_000017.11:35510833::AAA 15135/127926)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 35160892 (NC_000017.11:35510834::A 499/1832) Row 35160893 (NC_000017.11:35510834::AA 63/1832) Row 35160894 (NC_000017.11:35510834::AAA 368/1832)...	-	Apr 27, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 35160892 (NC_000017.11:35510834::A 499/1832) Row 35160893 (NC_000017.11:35510834::AA 63/1832) Row 35160894 (NC_000017.11:35510834::AAA 368/1832)...	-	Apr 27, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 35160892 (NC_000017.11:35510834::A 499/1832) Row 35160893 (NC_000017.11:35510834::AA 63/1832) Row 35160894 (NC_000017.11:35510834::AAA 368/1832)...	-	Apr 27, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 35160892 (NC_000017.11:35510834::A 499/1832) Row 35160893 (NC_000017.11:35510834::AA 63/1832) Row 35160894 (NC_000017.11:35510834::AAA 368/1832)...	-	Apr 27, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 35160892 (NC_000017.11:35510834::A 499/1832) Row 35160893 (NC_000017.11:35510834::AA 63/1832) Row 35160894 (NC_000017.11:35510834::AAA 368/1832)...	-	Apr 27, 2020 (154)
75	Northern Sweden Submission ignored due to conflicting rows: Row 15274455 (NC_000017.10:33837852::A 34/550) Row 15274456 (NC_000017.10:33837852::AA 87/550) Row 15274457 (NC_000017.10:33837852::AAA 14/550)	-	Jul 13, 2019 (153)
76	Northern Sweden Submission ignored due to conflicting rows: Row 15274455 (NC_000017.10:33837852::A 34/550) Row 15274456 (NC_000017.10:33837852::AA 87/550) Row 15274457 (NC_000017.10:33837852::AAA 14/550)	-	Jul 13, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 15274455 (NC_000017.10:33837852::A 34/550) Row 15274456 (NC_000017.10:33837852::AA 87/550) Row 15274457 (NC_000017.10:33837852::AAA 14/550)	-	Jul 13, 2019 (153)
78	8.3KJPN Submission ignored due to conflicting rows: Row 80156069 (NC_000017.10:33837852::A 4008/16740) Row 80156070 (NC_000017.10:33837852::AAA 4109/16740) Row 80156071 (NC_000017.10:33837852::AA 264/16740)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 80156069 (NC_000017.10:33837852::A 4008/16740) Row 80156070 (NC_000017.10:33837852::AAA 4109/16740) Row 80156071 (NC_000017.10:33837852::AA 264/16740)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 80156069 (NC_000017.10:33837852::A 4008/16740) Row 80156070 (NC_000017.10:33837852::AAA 4109/16740) Row 80156071 (NC_000017.10:33837852::AA 264/16740)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 80156069 (NC_000017.10:33837852::A 4008/16740) Row 80156070 (NC_000017.10:33837852::AAA 4109/16740) Row 80156071 (NC_000017.10:33837852::AA 264/16740)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 80156069 (NC_000017.10:33837852::A 4008/16740) Row 80156070 (NC_000017.10:33837852::AAA 4109/16740) Row 80156071 (NC_000017.10:33837852::AA 264/16740)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 80156069 (NC_000017.10:33837852::A 4008/16740) Row 80156070 (NC_000017.10:33837852::AAA 4109/16740) Row 80156071 (NC_000017.10:33837852::AA 264/16740)...	-	Apr 26, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 112157951 (NC_000017.11:35510833::A 6704/28258) Row 112157952 (NC_000017.11:35510833::AAA 7134/28258) Row 112157953 (NC_000017.11:35510833::AA 425/28258)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 112157951 (NC_000017.11:35510833::A 6704/28258) Row 112157952 (NC_000017.11:35510833::AAA 7134/28258) Row 112157953 (NC_000017.11:35510833::AA 425/28258)...	-	Oct 16, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 112157951 (NC_000017.11:35510833::A 6704/28258) Row 112157952 (NC_000017.11:35510833::AAA 7134/28258) Row 112157953 (NC_000017.11:35510833::AA 425/28258)...	-	Oct 16, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 112157951 (NC_000017.11:35510833::A 6704/28258) Row 112157952 (NC_000017.11:35510833::AAA 7134/28258) Row 112157953 (NC_000017.11:35510833::AA 425/28258)...	-	Oct 16, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 112157951 (NC_000017.11:35510833::A 6704/28258) Row 112157952 (NC_000017.11:35510833::AAA 7134/28258) Row 112157953 (NC_000017.11:35510833::AA 425/28258)...	-	Oct 16, 2022 (156)
89	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39750910 (NC_000017.10:33837852::AAA 423/3708) Row 39750911 (NC_000017.10:33837852::AA 732/3708)	-	Oct 12, 2018 (152)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39750910 (NC_000017.10:33837852::AAA 423/3708) Row 39750911 (NC_000017.10:33837852::AA 732/3708)	-	Oct 12, 2018 (152)
91	ALFA	NC_000017.11 - 35510834	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)
rs60177456	May 26, 2008 (130)
rs978955586	Nov 08, 2017 (151)
rs369006822	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4310734672	NC_000017.11:35510833:AAA:	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3700375964, ss4310734671, ss5302968894	NC_000017.11:35510833:AA:	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3015455632, ss5222186766	NC_000017.10:33837852:A:	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3978782894, ss4310734670, ss5302968892, ss5778320850	NC_000017.11:35510833:A:	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3700375963	NC_000017.11:35510834:A:	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss294910885	NC_000017.9:30861972::A	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3741989590, ss3834845936, ss5222186762	NC_000017.10:33837852::A	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4310734666, ss5302968889, ss5496049239, ss5778320847	NC_000017.11:35510833::A	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3978782891	NC_000017.11:35510834::A	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3700375962	NC_000017.11:35510835::A	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss40804724, ss79931080	NT_010799.15:8574859::A	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss664353390, ss1708740355, ss1708740438, ss3741989591, ss3793150823, ss3798036746, ss3841033187, ss5222186764, ss5833920850	NC_000017.10:33837852::AA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3846530238, ss4310734667, ss5302968891, ss5496049240, ss5778320849	NC_000017.11:35510833::AA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3978782892	NC_000017.11:35510834::AA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3700375961	NC_000017.11:35510835::AA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss666689736, ss1708740353, ss1708740437, ss3741989592, ss5222186763, ss5833920851	NC_000017.10:33837852::AAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4310734668, ss5302968890, ss5496049241, ss5778320848	NC_000017.11:35510833::AAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3978782893	NC_000017.11:35510834::AAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3700375960	NC_000017.11:35510835::AAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss79866882	NT_010799.15:8574859::AAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5222186765	NC_000017.10:33837852::AAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4310734669, ss5302968893, ss5496049242, ss5778320851	NC_000017.11:35510833::AAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3978782895	NC_000017.11:35510834::AAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3700375959	NC_000017.11:35510835::AAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5222186767	NC_000017.10:33837852::AAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8347725998	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000017.11:35510833:AAAAAAAAAAAA… NC_000017.11:35510833:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs34262146

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

rs34262146