Name: rs113809565
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.

rs113809565

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:109107863-109107875 (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)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.02032 (313/15401, ALFA)
dupA=0.070 (42/596, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CFAP276 : 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	15401	AAAAAAAAAAAAA=0.97968	AAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.02032, AAAAAAAAAAAAAAA=0.00000	0.962173	0.00286	0.034967	32
European	Sub	12557	AAAAAAAAAAAAA=0.97507	AAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.02493, AAAAAAAAAAAAAAA=0.00000	0.953596	0.003508	0.042896	32
African	Sub	2018	AAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	80	AAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1938	AAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	24	AAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	AAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	82	AAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	280	AAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	84	AAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	356	AAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	15401	(A)₁₃=0.97968	del(A)₄=0.00000, delAA=0.00000, delA=0.00000, dupA=0.02032, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	12557	(A)₁₃=0.97507	del(A)₄=0.00000, delAA=0.00000, delA=0.00000, dupA=0.02493, dupAA=0.00000
Allele Frequency Aggregator	African	Sub	2018	(A)₁₃=1.0000	del(A)₄=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Other	Sub	356	(A)₁₃=1.000	del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	280	(A)₁₃=1.000	del(A)₄=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	84	(A)₁₃=1.00	del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	82	(A)₁₃=1.00	del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	24	(A)₁₃=1.00	del(A)₄=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Northern Sweden	ACPOP	Study-wide	596	- No frequency provided	dupA=0.070

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 1	NC_000001.11:g.109107872_109107875del
GRCh38.p14 chr 1	NC_000001.11:g.109107873_109107875del
GRCh38.p14 chr 1	NC_000001.11:g.109107874_109107875del
GRCh38.p14 chr 1	NC_000001.11:g.109107875del
GRCh38.p14 chr 1	NC_000001.11:g.109107875dup
GRCh38.p14 chr 1	NC_000001.11:g.109107874_109107875dup
GRCh38.p14 chr 1	NC_000001.11:g.109107868_109107875dup
GRCh37.p13 chr 1	NC_000001.10:g.109650494_109650497del
GRCh37.p13 chr 1	NC_000001.10:g.109650495_109650497del
GRCh37.p13 chr 1	NC_000001.10:g.109650496_109650497del
GRCh37.p13 chr 1	NC_000001.10:g.109650497del
GRCh37.p13 chr 1	NC_000001.10:g.109650497dup
GRCh37.p13 chr 1	NC_000001.10:g.109650496_109650497dup
GRCh37.p13 chr 1	NC_000001.10:g.109650490_109650497dup

Gene: CFAP276, cilia and flagella associated protein 276 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CFAP276 transcript variant 3	NM_001122961.3:c.162+55_1… NM_001122961.3:c.162+55_162+58del	N/A	Intron Variant
CFAP276 transcript variant 1	NM_001245025.3:c.198+55_1… NM_001245025.3:c.198+55_198+58del	N/A	Intron Variant
CFAP276 transcript variant 2	NM_001366200.3:c.192+55_1… NM_001366200.3:c.192+55_192+58del	N/A	Intron Variant
CFAP276 transcript variant 4	NM_001366201.3:c.82-744_8… NM_001366201.3:c.82-744_82-741del	N/A	Intron Variant
CFAP276 transcript variant 5	NM_001366202.3:c.46-744_4… NM_001366202.3:c.46-744_46-741del	N/A	Intron Variant
CFAP276 transcript variant 6	NR_158762.3:n.	N/A	Intron Variant
CFAP276 transcript variant 7	NR_158763.3:n.	N/A	Intron Variant
CFAP276 transcript variant X1	XM_011540647.3:c.228+55_2… XM_011540647.3:c.228+55_228+58del	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=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₈
GRCh38.p14 chr 1	NC_000001.11:g.109107863_109107875=	NC_000001.11:g.109107872_109107875del	NC_000001.11:g.109107873_109107875del	NC_000001.11:g.109107874_109107875del	NC_000001.11:g.109107875del	NC_000001.11:g.109107875dup	NC_000001.11:g.109107874_109107875dup	NC_000001.11:g.109107868_109107875dup
GRCh37.p13 chr 1	NC_000001.10:g.109650485_109650497=	NC_000001.10:g.109650494_109650497del	NC_000001.10:g.109650495_109650497del	NC_000001.10:g.109650496_109650497del	NC_000001.10:g.109650497del	NC_000001.10:g.109650497dup	NC_000001.10:g.109650496_109650497dup	NC_000001.10:g.109650490_109650497dup
C1orf194 transcript variant 3	NM_001122961.1:c.162+58=	NM_001122961.1:c.162+55_162+58del	NM_001122961.1:c.162+56_162+58del	NM_001122961.1:c.162+57_162+58del	NM_001122961.1:c.162+58del	NM_001122961.1:c.162+58dup	NM_001122961.1:c.162+57_162+58dup	NM_001122961.1:c.162+51_162+58dup
CFAP276 transcript variant 3	NM_001122961.3:c.162+58=	NM_001122961.3:c.162+55_162+58del	NM_001122961.3:c.162+56_162+58del	NM_001122961.3:c.162+57_162+58del	NM_001122961.3:c.162+58del	NM_001122961.3:c.162+58dup	NM_001122961.3:c.162+57_162+58dup	NM_001122961.3:c.162+51_162+58dup
CFAP276 transcript variant 1	NM_001245025.3:c.198+58=	NM_001245025.3:c.198+55_198+58del	NM_001245025.3:c.198+56_198+58del	NM_001245025.3:c.198+57_198+58del	NM_001245025.3:c.198+58del	NM_001245025.3:c.198+58dup	NM_001245025.3:c.198+57_198+58dup	NM_001245025.3:c.198+51_198+58dup
CFAP276 transcript variant 2	NM_001366200.3:c.192+58=	NM_001366200.3:c.192+55_192+58del	NM_001366200.3:c.192+56_192+58del	NM_001366200.3:c.192+57_192+58del	NM_001366200.3:c.192+58del	NM_001366200.3:c.192+58dup	NM_001366200.3:c.192+57_192+58dup	NM_001366200.3:c.192+51_192+58dup
CFAP276 transcript variant 4	NM_001366201.3:c.82-741=	NM_001366201.3:c.82-744_82-741del	NM_001366201.3:c.82-743_82-741del	NM_001366201.3:c.82-742_82-741del	NM_001366201.3:c.82-741del	NM_001366201.3:c.82-741dup	NM_001366201.3:c.82-742_82-741dup	NM_001366201.3:c.82-748_82-741dup
CFAP276 transcript variant 5	NM_001366202.3:c.46-741=	NM_001366202.3:c.46-744_46-741del	NM_001366202.3:c.46-743_46-741del	NM_001366202.3:c.46-742_46-741del	NM_001366202.3:c.46-741del	NM_001366202.3:c.46-741dup	NM_001366202.3:c.46-742_46-741dup	NM_001366202.3:c.46-748_46-741dup
C1orf194 transcript variant X1	XM_005270448.1:c.46-741=	XM_005270448.1:c.46-744_46-741del	XM_005270448.1:c.46-743_46-741del	XM_005270448.1:c.46-742_46-741del	XM_005270448.1:c.46-741del	XM_005270448.1:c.46-741dup	XM_005270448.1:c.46-742_46-741dup	XM_005270448.1:c.46-748_46-741dup
CFAP276 transcript variant X1	XM_011540647.3:c.228+58=	XM_011540647.3:c.228+55_228+58del	XM_011540647.3:c.228+56_228+58del	XM_011540647.3:c.228+57_228+58del	XM_011540647.3:c.228+58del	XM_011540647.3:c.228+58dup	XM_011540647.3:c.228+57_228+58dup	XM_011540647.3:c.228+51_228+58dup

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#.

47 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193120898	Jul 04, 2010 (132)
2	GMI	ss288025607	May 04, 2012 (138)
3	SSMP	ss663108954	Apr 01, 2015 (144)
4	SSIP	ss947027973	Aug 21, 2014 (142)
5	HAMMER_LAB	ss1794909114	Sep 08, 2015 (146)
6	TMC_SNPDB	ss1997012948	Jul 19, 2016 (147)
7	SWEGEN	ss2987414746	Nov 08, 2017 (151)
8	MCHAISSO	ss3063603076	Nov 08, 2017 (151)
9	MCHAISSO	ss3064418398	Nov 08, 2017 (151)
10	EVA_DECODE	ss3687501594	Jul 12, 2019 (153)
11	EVA_DECODE	ss3687501595	Jul 12, 2019 (153)
12	EVA_DECODE	ss3687501596	Jul 12, 2019 (153)
13	EVA_DECODE	ss3687501597	Jul 12, 2019 (153)
14	ACPOP	ss3727376574	Jul 12, 2019 (153)
15	EVA	ss3826361747	Apr 25, 2020 (154)
16	EVA	ss3836572319	Apr 25, 2020 (154)
17	EVA	ss3841980632	Apr 25, 2020 (154)
18	KOGIC	ss3945216661	Apr 25, 2020 (154)
19	KOGIC	ss3945216662	Apr 25, 2020 (154)
20	KOGIC	ss3945216663	Apr 25, 2020 (154)
21	FSA-LAB	ss3983939491	Apr 25, 2021 (155)
22	FSA-LAB	ss3983939492	Apr 25, 2021 (155)
23	FSA-LAB	ss3983939493	Apr 25, 2021 (155)
24	GNOMAD	ss4000188086	Apr 25, 2021 (155)
25	GNOMAD	ss4000188087	Apr 25, 2021 (155)
26	GNOMAD	ss4000188088	Apr 25, 2021 (155)
27	GNOMAD	ss4000188089	Apr 25, 2021 (155)
28	TOPMED	ss4463091197	Apr 25, 2021 (155)
29	TOPMED	ss4463091198	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5145615882	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5145615883	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5145615884	Apr 25, 2021 (155)
33	GENOMICARE	ss5240820700	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5243560307	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5243560308	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5444488532	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5444488533	Oct 12, 2022 (156)
38	EVA	ss5623915526	Oct 12, 2022 (156)
39	EVA	ss5623995262	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5670864375	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5670864376	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5670864377	Oct 12, 2022 (156)
43	EVA	ss5800083748	Oct 12, 2022 (156)
44	EVA	ss5849062010	Oct 12, 2022 (156)
45	EVA	ss5909741789	Oct 12, 2022 (156)
46	EVA	ss5979977006	Oct 12, 2022 (156)
47	EVA	ss5981195542	Oct 12, 2022 (156)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22271917 (NC_000001.11:109107862::A 19941/124982) Row 22271918 (NC_000001.11:109107862::AA 33/125174) Row 22271919 (NC_000001.11:109107862:A: 341/124768)...	-	Apr 25, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22271917 (NC_000001.11:109107862::A 19941/124982) Row 22271918 (NC_000001.11:109107862::AA 33/125174) Row 22271919 (NC_000001.11:109107862:A: 341/124768)...	-	Apr 25, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22271917 (NC_000001.11:109107862::A 19941/124982) Row 22271918 (NC_000001.11:109107862::AA 33/125174) Row 22271919 (NC_000001.11:109107862:A: 341/124768)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22271917 (NC_000001.11:109107862::A 19941/124982) Row 22271918 (NC_000001.11:109107862::AA 33/125174) Row 22271919 (NC_000001.11:109107862:A: 341/124768)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22271917 (NC_000001.11:109107862::A 19941/124982) Row 22271918 (NC_000001.11:109107862::AA 33/125174) Row 22271919 (NC_000001.11:109107862:A: 341/124768)...	-	Apr 25, 2021 (155)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 1594662 (NC_000001.11:109107862:A: 79/1832) Row 1594663 (NC_000001.11:109107863::A 724/1832) Row 1594664 (NC_000001.11:109107863::AA 9/1832)	-	Apr 25, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 1594662 (NC_000001.11:109107862:A: 79/1832) Row 1594663 (NC_000001.11:109107863::A 724/1832) Row 1594664 (NC_000001.11:109107863::AA 9/1832)	-	Apr 25, 2020 (154)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 1594662 (NC_000001.11:109107862:A: 79/1832) Row 1594663 (NC_000001.11:109107863::A 724/1832) Row 1594664 (NC_000001.11:109107863::AA 9/1832)	-	Apr 25, 2020 (154)
56	Northern Sweden	NC_000001.10 - 109650485	Jul 12, 2019 (153)
57	8.3KJPN Submission ignored due to conflicting rows: Row 3585189 (NC_000001.10:109650484::A 7789/16744) Row 3585190 (NC_000001.10:109650484:A: 22/16744) Row 3585191 (NC_000001.10:109650484::AA 20/16744)	-	Apr 25, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 3585189 (NC_000001.10:109650484::A 7789/16744) Row 3585190 (NC_000001.10:109650484:A: 22/16744) Row 3585191 (NC_000001.10:109650484::AA 20/16744)	-	Apr 25, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 3585189 (NC_000001.10:109650484::A 7789/16744) Row 3585190 (NC_000001.10:109650484:A: 22/16744) Row 3585191 (NC_000001.10:109650484::AA 20/16744)	-	Apr 25, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 4701479 (NC_000001.11:109107862::A 13085/28254) Row 4701480 (NC_000001.11:109107862:A: 36/28254) Row 4701481 (NC_000001.11:109107862::AA 29/28254)	-	Oct 12, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 4701479 (NC_000001.11:109107862::A 13085/28254) Row 4701480 (NC_000001.11:109107862:A: 36/28254) Row 4701481 (NC_000001.11:109107862::AA 29/28254)	-	Oct 12, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 4701479 (NC_000001.11:109107862::A 13085/28254) Row 4701480 (NC_000001.11:109107862:A: 36/28254) Row 4701481 (NC_000001.11:109107862::AA 29/28254)	-	Oct 12, 2022 (156)
63	TopMed Submission ignored due to conflicting rows: Row 26697532 (NC_000001.11:109107862:AA: 1/264690) Row 26697533 (NC_000001.11:109107862:AAAA: 2/264690)	-	Apr 25, 2021 (155)
64	TopMed Submission ignored due to conflicting rows: Row 26697532 (NC_000001.11:109107862:AA: 1/264690) Row 26697533 (NC_000001.11:109107862:AAAA: 2/264690)	-	Apr 25, 2021 (155)
65	ALFA	NC_000001.11 - 109107863	Apr 25, 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)
rs202220180	May 15, 2013 (138)
rs369571562	May 15, 2013 (138)
rs1010809841	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4463091198	NC_000001.11:109107862:AAAA:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAA	(self)
235391127	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4000188089	NC_000001.11:109107862:AAA:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3983939492, ss3983939493	NC_000001.10:109650484:AA:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3687501597, ss4000188088, ss4463091197	NC_000001.11:109107862:AA:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
235391127	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss1997012948, ss5145615883, ss5240820700, ss5623915526, ss5623995262, ss5981195542	NC_000001.10:109650484:A:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3945216661, ss5243560308, ss5444488533, ss5670864376	NC_000001.11:109107862:A:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
235391127	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3687501596	NC_000001.11:109107863:A:	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss288025607	NC_000001.9:109452020::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
661439, ss663108954, ss1794909114, ss2987414746, ss3727376574, ss3826361747, ss3836572319, ss3983939491, ss5145615882, ss5800083748, ss5979977006	NC_000001.10:109650484::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss947027973	NC_000001.10:109650485::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3063603076, ss3064418398, ss3841980632, ss4000188086, ss5243560307, ss5444488532, ss5670864375, ss5849062010, ss5909741789	NC_000001.11:109107862::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
235391127	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3945216662	NC_000001.11:109107863::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3687501595	NC_000001.11:109107864::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss193120898	NT_032977.10:108521874::A	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5145615884	NC_000001.10:109650484::AA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4000188087, ss5670864377	NC_000001.11:109107862::AA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
235391127	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3945216663	NC_000001.11:109107863::AA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3687501594	NC_000001.11:109107864::AAAAAAAA	NC_000001.11:109107862:AAAAAAAAAAA… NC_000001.11:109107862:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(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 rs113809565

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

rs113809565