Name: rs35961208
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.

rs35961208

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:40048615-40048629 (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
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₅=0.4107 (2057/5008, 1000G)
delAAA=0.0000 (0/1592, ALFA)
delAA=0.0000 (0/1592, ALFA) (+ 4 more)
delA=0.0000 (0/1592, ALFA)
dupA=0.0000 (0/1592, ALFA)
dupAA=0.0000 (0/1592, ALFA)
(A)₁₅=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC344967 : 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	1592	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	564	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	856	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	36	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	820	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	14	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	62	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	68	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.4107	delAA=0.5893
1000Genomes	African	Sub	1322	(A)₁₅=0.6694	delAA=0.3306
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.3165	delAA=0.6835
1000Genomes	Europe	Sub	1006	(A)₁₅=0.2694	delAA=0.7306
1000Genomes	South Asian	Sub	978	(A)₁₅=0.345	delAA=0.655
1000Genomes	American	Sub	694	(A)₁₅=0.353	delAA=0.647
Allele Frequency Aggregator	Total	Global	1592	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	856	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	564	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	68	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	62	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	16	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₅=0.23	delAA=0.78

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 4	NC_000004.12:g.40048626_40048629del
GRCh38.p14 chr 4	NC_000004.12:g.40048627_40048629del
GRCh38.p14 chr 4	NC_000004.12:g.40048628_40048629del
GRCh38.p14 chr 4	NC_000004.12:g.40048629del
GRCh38.p14 chr 4	NC_000004.12:g.40048629dup
GRCh38.p14 chr 4	NC_000004.12:g.40048628_40048629dup
GRCh37.p13 chr 4	NC_000004.11:g.40050246_40050249del
GRCh37.p13 chr 4	NC_000004.11:g.40050247_40050249del
GRCh37.p13 chr 4	NC_000004.11:g.40050248_40050249del
GRCh37.p13 chr 4	NC_000004.11:g.40050249del
GRCh37.p13 chr 4	NC_000004.11:g.40050249dup
GRCh37.p13 chr 4	NC_000004.11:g.40050248_40050249dup

Gene: LOC344967, acyl-CoA thioesterase 7 pseudogene (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC344967 transcript	NR_027277.2: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)₁₅=	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 4	NC_000004.12:g.40048615_40048629=	NC_000004.12:g.40048626_40048629del	NC_000004.12:g.40048627_40048629del	NC_000004.12:g.40048628_40048629del	NC_000004.12:g.40048629del	NC_000004.12:g.40048629dup	NC_000004.12:g.40048628_40048629dup
GRCh37.p13 chr 4	NC_000004.11:g.40050235_40050249=	NC_000004.11:g.40050246_40050249del	NC_000004.11:g.40050247_40050249del	NC_000004.11:g.40050248_40050249del	NC_000004.11:g.40050249del	NC_000004.11:g.40050249dup	NC_000004.11:g.40050248_40050249dup

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#.

54 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42305324	Dec 03, 2013 (138)
2	HGSV	ss81991730	Dec 14, 2007 (137)
3	HUMANGENOME_JCVI	ss98909144	Dec 03, 2013 (138)
4	GMI	ss288511280	May 04, 2012 (137)
5	PJP	ss295161455	May 09, 2011 (134)
6	SSMP	ss663508417	Apr 01, 2015 (144)
7	1000GENOMES	ss1372062101	Aug 21, 2014 (142)
8	DDI	ss1536403639	Apr 01, 2015 (144)
9	EVA_GENOME_DK	ss1576213903	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1704125109	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1704125653	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1710142566	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710142577	Apr 01, 2015 (144)
14	HAMMER_LAB	ss1801309869	Sep 08, 2015 (146)
15	SWEGEN	ss2994498643	Nov 08, 2017 (151)
16	MCHAISSO	ss3064097493	Nov 08, 2017 (151)
17	MCHAISSO	ss3064963628	Nov 08, 2017 (151)
18	BIOINF_KMB_FNS_UNIBA	ss3645788778	Oct 12, 2018 (152)
19	URBANLAB	ss3647702923	Oct 12, 2018 (152)
20	EVA_DECODE	ss3711848904	Jul 13, 2019 (153)
21	EVA_DECODE	ss3711848905	Jul 13, 2019 (153)
22	EVA_DECODE	ss3711848906	Jul 13, 2019 (153)
23	EVA_DECODE	ss3711848907	Jul 13, 2019 (153)
24	PACBIO	ss3784682919	Jul 13, 2019 (153)
25	PACBIO	ss3790145448	Jul 13, 2019 (153)
26	PACBIO	ss3795020641	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3804809476	Jul 13, 2019 (153)
28	EVA	ss3828488097	Apr 26, 2020 (154)
29	GNOMAD	ss4094335552	Apr 26, 2021 (155)
30	GNOMAD	ss4094335553	Apr 26, 2021 (155)
31	GNOMAD	ss4094335554	Apr 26, 2021 (155)
32	GNOMAD	ss4094335555	Apr 26, 2021 (155)
33	GNOMAD	ss4094335556	Apr 26, 2021 (155)
34	GNOMAD	ss4094335557	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5165183417	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5165183418	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5165183419	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5165183420	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5258821762	Oct 13, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5258821763	Oct 13, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5258821764	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5258821765	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5457645518	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5457645519	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5457645520	Oct 13, 2022 (156)
46	EVA	ss5507474519	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5699102104	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5699102105	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5699102106	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5699102107	Oct 13, 2022 (156)
51	EVA	ss5843854607	Oct 13, 2022 (156)
52	EVA	ss5843854608	Oct 13, 2022 (156)
53	EVA	ss5854180515	Oct 13, 2022 (156)
54	EVA	ss5980218628	Oct 13, 2022 (156)
55	1000Genomes	NC_000004.11 - 40050235	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11532536 (NC_000004.11:40050235:A: 2965/3854) Row 11532537 (NC_000004.11:40050234:AAA: 209/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 11532536 (NC_000004.11:40050235:A: 2965/3854) Row 11532537 (NC_000004.11:40050234:AAA: 209/3854)	-	Oct 12, 2018 (152)
58	The Danish reference pan genome	NC_000004.11 - 40050235	Apr 26, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146547909 (NC_000004.12:40048614::A 267/120562) Row 146547910 (NC_000004.12:40048614::AA 2/120594) Row 146547911 (NC_000004.12:40048614:A: 5239/120452)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146547909 (NC_000004.12:40048614::A 267/120562) Row 146547910 (NC_000004.12:40048614::AA 2/120594) Row 146547911 (NC_000004.12:40048614:A: 5239/120452)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146547909 (NC_000004.12:40048614::A 267/120562) Row 146547910 (NC_000004.12:40048614::AA 2/120594) Row 146547911 (NC_000004.12:40048614:A: 5239/120452)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146547909 (NC_000004.12:40048614::A 267/120562) Row 146547910 (NC_000004.12:40048614::AA 2/120594) Row 146547911 (NC_000004.12:40048614:A: 5239/120452)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146547909 (NC_000004.12:40048614::A 267/120562) Row 146547910 (NC_000004.12:40048614::AA 2/120594) Row 146547911 (NC_000004.12:40048614:A: 5239/120452)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 146547909 (NC_000004.12:40048614::A 267/120562) Row 146547910 (NC_000004.12:40048614::AA 2/120594) Row 146547911 (NC_000004.12:40048614:A: 5239/120452)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 23152724 (NC_000004.11:40050234:AA: 12232/16520) Row 23152725 (NC_000004.11:40050234:A: 144/16520) Row 23152726 (NC_000004.11:40050234:AAA: 13/16520)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 23152724 (NC_000004.11:40050234:AA: 12232/16520) Row 23152725 (NC_000004.11:40050234:A: 144/16520) Row 23152726 (NC_000004.11:40050234:AAA: 13/16520)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 23152724 (NC_000004.11:40050234:AA: 12232/16520) Row 23152725 (NC_000004.11:40050234:A: 144/16520) Row 23152726 (NC_000004.11:40050234:AAA: 13/16520)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 23152724 (NC_000004.11:40050234:AA: 12232/16520) Row 23152725 (NC_000004.11:40050234:A: 144/16520) Row 23152726 (NC_000004.11:40050234:AAA: 13/16520)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 32939208 (NC_000004.12:40048614:AA: 20658/27998) Row 32939209 (NC_000004.12:40048614:A: 234/27998) Row 32939210 (NC_000004.12:40048614:AAA: 16/27998)...	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 32939208 (NC_000004.12:40048614:AA: 20658/27998) Row 32939209 (NC_000004.12:40048614:A: 234/27998) Row 32939210 (NC_000004.12:40048614:AAA: 16/27998)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 32939208 (NC_000004.12:40048614:AA: 20658/27998) Row 32939209 (NC_000004.12:40048614:A: 234/27998) Row 32939210 (NC_000004.12:40048614:AAA: 16/27998)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 32939208 (NC_000004.12:40048614:AA: 20658/27998) Row 32939209 (NC_000004.12:40048614:A: 234/27998) Row 32939210 (NC_000004.12:40048614:AAA: 16/27998)...	-	Oct 13, 2022 (156)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11532536 (NC_000004.11:40050235:A: 2855/3708) Row 11532537 (NC_000004.11:40050234:AAA: 175/3708)	-	Oct 12, 2018 (152)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 11532536 (NC_000004.11:40050235:A: 2855/3708) Row 11532537 (NC_000004.11:40050234:AAA: 175/3708)	-	Oct 12, 2018 (152)
75	ALFA	NC_000004.12 - 40048615	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)
rs56822513	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4094335557	NC_000004.12:40048614:AAAA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss1704125109, ss1704125653, ss5165183419, ss5843854608	NC_000004.11:40050234:AAA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3711848907, ss4094335556, ss5258821764, ss5699102106	NC_000004.12:40048614:AAA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
11172134184	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss81991730	NC_000004.9:39872813:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss288511280, ss295161455	NC_000004.10:39726642:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
20698235, 904379, ss663508417, ss1372062101, ss1536403639, ss1576213903, ss1801309869, ss2994498643, ss3784682919, ss3790145448, ss3795020641, ss3828488097, ss5165183417, ss5843854607, ss5980218628	NC_000004.11:40050234:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710142566, ss1710142577	NC_000004.11:40050235:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3064097493, ss3064963628, ss3645788778, ss3647702923, ss3804809476, ss4094335555, ss5258821762, ss5457645518, ss5699102104, ss5854180515	NC_000004.12:40048614:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
11172134184	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3711848906	NC_000004.12:40048615:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss42305324, ss98909144	NT_016297.16:7209596:AA:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5165183418	NC_000004.11:40050234:A:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
	NC_000004.11:40050235:A:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4094335554, ss5258821763, ss5457645519, ss5699102105	NC_000004.12:40048614:A:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
11172134184	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3711848905	NC_000004.12:40048616:A:	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5165183420	NC_000004.11:40050234::A	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4094335552, ss5258821765, ss5457645520, ss5699102107	NC_000004.12:40048614::A	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
11172134184	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3711848904	NC_000004.12:40048617::A	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5507474519	NC_000004.11:40050234::AA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA
ss4094335553	NC_000004.12:40048614::AA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
11172134184	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000004.12:40048614:AAAAAAAAAAAA… NC_000004.12:40048614:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(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 rs35961208

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

rs35961208