Name: rs35795789
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.

rs35795789

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:26352844-26352859 (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 / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.0000 (0/6926, ALFA)
delAA=0.0000 (0/6926, ALFA)
delA=0.0000 (0/6926, ALFA) (+ 6 more)
dupA=0.0000 (0/6926, ALFA)
dupAA=0.0000 (0/6926, ALFA)
dupAAA=0.0000 (0/6926, ALFA)
dup(A)₄=0.0000 (0/6926, ALFA)
dup(A)₇=0.0000 (0/6926, ALFA)
dupA=0.3099 (1552/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SELENOI : 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	HWEP
Total	Global	6926	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	4834	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1510	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	52	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1458	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	46	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	36	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	50	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	246	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	36	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	204	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6926	(A)₁₆=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	European	Sub	4834	(A)₁₆=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	African	Sub	1510	(A)₁₆=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	246	(A)₁₆=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Other	Sub	204	(A)₁₆=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(A)₁₆=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Asian	Sub	46	(A)₁₆=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	36	(A)₁₆=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₇=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.3099
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.2390
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.2956
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.3390
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.395
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.304

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 2	NC_000002.12:g.26352857_26352859del
GRCh38.p14 chr 2	NC_000002.12:g.26352858_26352859del
GRCh38.p14 chr 2	NC_000002.12:g.26352859del
GRCh38.p14 chr 2	NC_000002.12:g.26352859dup
GRCh38.p14 chr 2	NC_000002.12:g.26352858_26352859dup
GRCh38.p14 chr 2	NC_000002.12:g.26352857_26352859dup
GRCh38.p14 chr 2	NC_000002.12:g.26352856_26352859dup
GRCh38.p14 chr 2	NC_000002.12:g.26352855_26352859dup
GRCh38.p14 chr 2	NC_000002.12:g.26352853_26352859dup
GRCh37.p13 chr 2	NC_000002.11:g.26575725_26575727del
GRCh37.p13 chr 2	NC_000002.11:g.26575726_26575727del
GRCh37.p13 chr 2	NC_000002.11:g.26575727del
GRCh37.p13 chr 2	NC_000002.11:g.26575727dup
GRCh37.p13 chr 2	NC_000002.11:g.26575726_26575727dup
GRCh37.p13 chr 2	NC_000002.11:g.26575725_26575727dup
GRCh37.p13 chr 2	NC_000002.11:g.26575724_26575727dup
GRCh37.p13 chr 2	NC_000002.11:g.26575723_26575727dup
GRCh37.p13 chr 2	NC_000002.11:g.26575721_26575727dup

Gene: SELENOI, selenoprotein I (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SELENOI transcript variant 1	NM_033505.4:c.57+6568_57+… NM_033505.4:c.57+6568_57+6570del	N/A	Intron Variant
SELENOI transcript variant 2	NR_137633.2: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)₁₆=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₇
GRCh38.p14 chr 2	NC_000002.12:g.26352844_26352859=	NC_000002.12:g.26352857_26352859del	NC_000002.12:g.26352858_26352859del	NC_000002.12:g.26352859del	NC_000002.12:g.26352859dup	NC_000002.12:g.26352858_26352859dup	NC_000002.12:g.26352857_26352859dup	NC_000002.12:g.26352856_26352859dup	NC_000002.12:g.26352855_26352859dup	NC_000002.12:g.26352853_26352859dup
GRCh37.p13 chr 2	NC_000002.11:g.26575712_26575727=	NC_000002.11:g.26575725_26575727del	NC_000002.11:g.26575726_26575727del	NC_000002.11:g.26575727del	NC_000002.11:g.26575727dup	NC_000002.11:g.26575726_26575727dup	NC_000002.11:g.26575725_26575727dup	NC_000002.11:g.26575724_26575727dup	NC_000002.11:g.26575723_26575727dup	NC_000002.11:g.26575721_26575727dup
EPT1 transcript	NM_033505.2:c.57+6555=	NM_033505.2:c.57+6568_57+6570del	NM_033505.2:c.57+6569_57+6570del	NM_033505.2:c.57+6570del	NM_033505.2:c.57+6570dup	NM_033505.2:c.57+6569_57+6570dup	NM_033505.2:c.57+6568_57+6570dup	NM_033505.2:c.57+6567_57+6570dup	NM_033505.2:c.57+6566_57+6570dup	NM_033505.2:c.57+6564_57+6570dup
SELENOI transcript variant 1	NM_033505.4:c.57+6555=	NM_033505.4:c.57+6568_57+6570del	NM_033505.4:c.57+6569_57+6570del	NM_033505.4:c.57+6570del	NM_033505.4:c.57+6570dup	NM_033505.4:c.57+6569_57+6570dup	NM_033505.4:c.57+6568_57+6570dup	NM_033505.4:c.57+6567_57+6570dup	NM_033505.4:c.57+6566_57+6570dup	NM_033505.4:c.57+6564_57+6570dup

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#.

43 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41779206	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95267327	Feb 06, 2009 (130)
3	GMI	ss288143196	May 04, 2012 (137)
4	PJP	ss294976733	May 09, 2011 (137)
5	PJP	ss294976734	May 09, 2011 (135)
6	SSMP	ss663299460	Apr 01, 2015 (144)
7	SSIP	ss947048577	Aug 21, 2014 (142)
8	1000GENOMES	ss1368148166	Aug 21, 2014 (142)
9	SWEGEN	ss2989161431	Nov 08, 2017 (151)
10	MCHAISSO	ss3065731950	Nov 08, 2017 (151)
11	EVA_DECODE	ss3703475469	Jul 12, 2019 (153)
12	EVA_DECODE	ss3703475470	Jul 12, 2019 (153)
13	EVA_DECODE	ss3703475471	Jul 12, 2019 (153)
14	PACBIO	ss3783809471	Jul 12, 2019 (153)
15	PACBIO	ss3794278537	Jul 12, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3800876637	Jul 12, 2019 (153)
17	EVA	ss3826877216	Apr 25, 2020 (154)
18	EVA	ss3836845701	Apr 25, 2020 (154)
19	EVA	ss3842260270	Apr 25, 2020 (154)
20	GNOMAD	ss4037504142	Apr 26, 2021 (155)
21	GNOMAD	ss4037504143	Apr 26, 2021 (155)
22	GNOMAD	ss4037504144	Apr 26, 2021 (155)
23	GNOMAD	ss4037504145	Apr 26, 2021 (155)
24	GNOMAD	ss4037504146	Apr 26, 2021 (155)
25	GNOMAD	ss4037504147	Apr 26, 2021 (155)
26	GNOMAD	ss4037504148	Apr 26, 2021 (155)
27	GNOMAD	ss4037504149	Apr 26, 2021 (155)
28	GNOMAD	ss4037504150	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5150384812	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5150384813	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5150384814	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5247312891	Oct 17, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5247312893	Oct 17, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5247312894	Oct 17, 2022 (156)
35	HUGCELL_USP	ss5447584749	Oct 17, 2022 (156)
36	HUGCELL_USP	ss5447584750	Oct 17, 2022 (156)
37	HUGCELL_USP	ss5447584751	Oct 17, 2022 (156)
38	TOMMO_GENOMICS	ss5678725269	Oct 17, 2022 (156)
39	TOMMO_GENOMICS	ss5678725270	Oct 17, 2022 (156)
40	TOMMO_GENOMICS	ss5678725271	Oct 17, 2022 (156)
41	EVA	ss5819810486	Oct 17, 2022 (156)
42	EVA	ss5819810487	Oct 17, 2022 (156)
43	EVA	ss5852437236	Oct 17, 2022 (156)
44	1000Genomes	NC_000002.11 - 26575712	Oct 11, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 51752928 (NC_000002.12:26352843::A 44924/116386) Row 51752929 (NC_000002.12:26352843::AA 198/116556) Row 51752930 (NC_000002.12:26352843::AAA 5/116648)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 8354119 (NC_000002.11:26575711::A 3183/16754) Row 8354120 (NC_000002.11:26575711:A: 25/16754) Row 8354121 (NC_000002.11:26575711::AA 7/16754)	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 8354119 (NC_000002.11:26575711::A 3183/16754) Row 8354120 (NC_000002.11:26575711:A: 25/16754) Row 8354121 (NC_000002.11:26575711::AA 7/16754)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 8354119 (NC_000002.11:26575711::A 3183/16754) Row 8354120 (NC_000002.11:26575711:A: 25/16754) Row 8354121 (NC_000002.11:26575711::AA 7/16754)	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 12562373 (NC_000002.12:26352843::A 5471/28258) Row 12562374 (NC_000002.12:26352843:A: 35/28258) Row 12562375 (NC_000002.12:26352843::AA 14/28258)	-	Oct 17, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 12562373 (NC_000002.12:26352843::A 5471/28258) Row 12562374 (NC_000002.12:26352843:A: 35/28258) Row 12562375 (NC_000002.12:26352843::AA 14/28258)	-	Oct 17, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 12562373 (NC_000002.12:26352843::A 5471/28258) Row 12562374 (NC_000002.12:26352843:A: 35/28258) Row 12562375 (NC_000002.12:26352843::AA 14/28258)	-	Oct 17, 2022 (156)
60	ALFA	NC_000002.12 - 26352844	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)
rs72329705	May 11, 2012 (137)
rs140237642	May 11, 2012 (137)
rs145872241	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4037504150	NC_000002.12:26352843:AAA:	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4037504149	NC_000002.12:26352843:AA:	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5150384813	NC_000002.11:26575711:A:	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3065731950, ss3703475471, ss4037504148, ss5247312893, ss5447584751, ss5678725270	NC_000002.12:26352843:A:	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss294976733	NC_000002.10:26429216::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss288143196, ss294976734	NC_000002.10:26429231::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7283692, ss663299460, ss1368148166, ss2989161431, ss3783809471, ss3794278537, ss3826877216, ss3836845701, ss5150384812, ss5819810486	NC_000002.11:26575711::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss947048577	NC_000002.11:26575712::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3800876637, ss3842260270, ss4037504142, ss5247312891, ss5447584749, ss5678725269, ss5852437236	NC_000002.12:26352843::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3703475470	NC_000002.12:26352844::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss41779206, ss95267327	NT_022184.15:5397614::A	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5150384814, ss5819810487	NC_000002.11:26575711::AA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4037504143, ss5247312894, ss5447584750, ss5678725271	NC_000002.12:26352843::AA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3703475469	NC_000002.12:26352844::AA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4037504144	NC_000002.12:26352843::AAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4037504145	NC_000002.12:26352843::AAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4037504146	NC_000002.12:26352843::AAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4037504147	NC_000002.12:26352843::AAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
12046170929	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000002.12:26352843:AAAAAAAAAAAA… NC_000002.12:26352843:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(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 rs35795789

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

rs35795789