Name: rs35152391
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.

rs35152391

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:96999862-96999879 (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(GC)₆ / del(GC)₅ / del(GC)₄ / d…
del(GC)₆ / del(GC)₅ / del(GC)₄ / del(GC)₃ / delGCGC / delGC / dupGC / dupGCGC
Variation Type: Indel Insertion and Deletion
Frequency: dupGC=0.000015 (4/264690, TOPMED)
del(GC)₆=0.0000 (0/5304, ALFA)
del(GC)₅=0.0000 (0/5304, ALFA) (+ 6 more)
del(GC)₄=0.0000 (0/5304, ALFA)
del(GC)₃=0.0000 (0/5304, ALFA)
delGCGC=0.0000 (0/5304, ALFA)
delGC=0.0000 (0/5304, ALFA)
dupGC=0.0000 (0/5304, ALFA)
dupGCGC=0.0000 (0/5304, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DLX6-AS1 : 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	5304	GCGCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
European	Sub	3470	GCGCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
African	Sub	1322	GCGCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
African Others	Sub	38	GCGCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
African American	Sub	1284	GCGCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
Asian	Sub	66	GCGCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
East Asian	Sub	50	GCGCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Other Asian	Sub	16	GCGCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Latin American 1	Sub	44	GCGCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Latin American 2	Sub	168	GCGCGCGCGCGCGCGCGC=1.000	GCGCGC=0.000, GCGCGCGC=0.000, GCGCGCGCGC=0.000, GCGCGCGCGCGC=0.000, GCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGC=0.000	1.0	N/A
South Asian	Sub	48	GCGCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Other	Sub	186	GCGCGCGCGCGCGCGCGC=1.000	GCGCGC=0.000, GCGCGCGC=0.000, GCGCGCGCGC=0.000, GCGCGCGCGCGC=0.000, GCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGC=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	- No frequency provided	dupGC=0.000015
Allele Frequency Aggregator	Total	Global	5304	(GC)₉=1.0000	del(GC)₆=0.0000, del(GC)₅=0.0000, del(GC)₄=0.0000, del(GC)₃=0.0000, delGCGC=0.0000, delGC=0.0000, dupGC=0.0000, dupGCGC=0.0000
Allele Frequency Aggregator	European	Sub	3470	(GC)₉=1.0000	del(GC)₆=0.0000, del(GC)₅=0.0000, del(GC)₄=0.0000, del(GC)₃=0.0000, delGCGC=0.0000, delGC=0.0000, dupGC=0.0000, dupGCGC=0.0000
Allele Frequency Aggregator	African	Sub	1322	(GC)₉=1.0000	del(GC)₆=0.0000, del(GC)₅=0.0000, del(GC)₄=0.0000, del(GC)₃=0.0000, delGCGC=0.0000, delGC=0.0000, dupGC=0.0000, dupGCGC=0.0000
Allele Frequency Aggregator	Other	Sub	186	(GC)₉=1.000	del(GC)₆=0.000, del(GC)₅=0.000, del(GC)₄=0.000, del(GC)₃=0.000, delGCGC=0.000, delGC=0.000, dupGC=0.000, dupGCGC=0.000
Allele Frequency Aggregator	Latin American 2	Sub	168	(GC)₉=1.000	del(GC)₆=0.000, del(GC)₅=0.000, del(GC)₄=0.000, del(GC)₃=0.000, delGCGC=0.000, delGC=0.000, dupGC=0.000, dupGCGC=0.000
Allele Frequency Aggregator	Asian	Sub	66	(GC)₉=1.00	del(GC)₆=0.00, del(GC)₅=0.00, del(GC)₄=0.00, del(GC)₃=0.00, delGCGC=0.00, delGC=0.00, dupGC=0.00, dupGCGC=0.00
Allele Frequency Aggregator	South Asian	Sub	48	(GC)₉=1.00	del(GC)₆=0.00, del(GC)₅=0.00, del(GC)₄=0.00, del(GC)₃=0.00, delGCGC=0.00, delGC=0.00, dupGC=0.00, dupGCGC=0.00
Allele Frequency Aggregator	Latin American 1	Sub	44	(GC)₉=1.00	del(GC)₆=0.00, del(GC)₅=0.00, del(GC)₄=0.00, del(GC)₃=0.00, delGCGC=0.00, delGC=0.00, dupGC=0.00, dupGCGC=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 7	NC_000007.14:g.96999862GC[3]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[4]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[5]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[6]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[7]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[8]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[10]
GRCh38.p14 chr 7	NC_000007.14:g.96999862GC[11]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[3]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[4]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[5]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[6]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[7]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[8]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[10]
GRCh37.p13 chr 7	NC_000007.13:g.96629174GC[11]

Gene: DLX6-AS1, DLX6 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DLX6-AS1 transcript	NR_015448.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(GC)₉=	del(GC)₆	del(GC)₅	del(GC)₄	del(GC)₃	delGCGC	delGC	dupGC	dupGCGC
GRCh38.p14 chr 7	NC_000007.14:g.96999862_96999879=	NC_000007.14:g.96999862GC[3]	NC_000007.14:g.96999862GC[4]	NC_000007.14:g.96999862GC[5]	NC_000007.14:g.96999862GC[6]	NC_000007.14:g.96999862GC[7]	NC_000007.14:g.96999862GC[8]	NC_000007.14:g.96999862GC[10]	NC_000007.14:g.96999862GC[11]
GRCh37.p13 chr 7	NC_000007.13:g.96629174_96629191=	NC_000007.13:g.96629174GC[3]	NC_000007.13:g.96629174GC[4]	NC_000007.13:g.96629174GC[5]	NC_000007.13:g.96629174GC[6]	NC_000007.13:g.96629174GC[7]	NC_000007.13:g.96629174GC[8]	NC_000007.13:g.96629174GC[10]	NC_000007.13:g.96629174GC[11]

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#.

29 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80872919	Jan 10, 2018 (151)
2	1000GENOMES	ss326966442	Sep 08, 2015 (146)
3	DDI	ss1536556521	Sep 08, 2015 (146)
4	BEROUKHIMLAB	ss3644244267	Oct 12, 2018 (152)
5	EVA_DECODE	ss3720261714	Jul 13, 2019 (153)
6	EVA_DECODE	ss3720261719	Jul 13, 2019 (153)
7	PACBIO	ss3785900123	Jul 13, 2019 (153)
8	PACBIO	ss3791189438	Jul 13, 2019 (153)
9	PACBIO	ss3796069431	Jul 13, 2019 (153)
10	KOGIC	ss3962145773	Apr 26, 2020 (154)
11	KOGIC	ss3962145774	Apr 26, 2020 (154)
12	GNOMAD	ss4169031784	Apr 26, 2021 (155)
13	GNOMAD	ss4169031785	Apr 26, 2021 (155)
14	GNOMAD	ss4169031786	Apr 26, 2021 (155)
15	GNOMAD	ss4169031787	Apr 26, 2021 (155)
16	GNOMAD	ss4169031788	Apr 26, 2021 (155)
17	GNOMAD	ss4169031789	Apr 26, 2021 (155)
18	GNOMAD	ss4169031790	Apr 26, 2021 (155)
19	GNOMAD	ss4169031791	Apr 26, 2021 (155)
20	TOPMED	ss4755915790	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5184569952	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5184569953	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5184569954	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5184569955	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5273961838	Oct 13, 2022 (156)
26	HUGCELL_USP	ss5470941666	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5725250028	Oct 13, 2022 (156)
28	TOMMO_GENOMICS	ss5725250029	Oct 13, 2022 (156)
29	TOMMO_GENOMICS	ss5725250031	Oct 13, 2022 (156)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 270074829 (NC_000007.14:96999861::GC 5/124026) Row 270074830 (NC_000007.14:96999861::GCGC 1/124026) Row 270074831 (NC_000007.14:96999861:GC: 45005/123980)...	-	Apr 26, 2021 (155)
38	Korean Genome Project Submission ignored due to conflicting rows: Row 18523774 (NC_000007.14:96999865:GC: 579/1830) Row 18523775 (NC_000007.14:96999861:GCGCGC: 25/1830)	-	Apr 26, 2020 (154)
39	Korean Genome Project Submission ignored due to conflicting rows: Row 18523774 (NC_000007.14:96999865:GC: 579/1830) Row 18523775 (NC_000007.14:96999861:GCGCGC: 25/1830)	-	Apr 26, 2020 (154)
40	8.3KJPN Submission ignored due to conflicting rows: Row 42539259 (NC_000007.13:96629173:GC: 5669/16734) Row 42539260 (NC_000007.13:96629173:GCGCGC: 417/16734) Row 42539261 (NC_000007.13:96629173::GC 2/16734)...	-	Apr 26, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 42539259 (NC_000007.13:96629173:GC: 5669/16734) Row 42539260 (NC_000007.13:96629173:GCGCGC: 417/16734) Row 42539261 (NC_000007.13:96629173::GC 2/16734)...	-	Apr 26, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 42539259 (NC_000007.13:96629173:GC: 5669/16734) Row 42539260 (NC_000007.13:96629173:GCGCGC: 417/16734) Row 42539261 (NC_000007.13:96629173::GC 2/16734)...	-	Apr 26, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 42539259 (NC_000007.13:96629173:GC: 5669/16734) Row 42539260 (NC_000007.13:96629173:GCGCGC: 417/16734) Row 42539261 (NC_000007.13:96629173::GC 2/16734)...	-	Apr 26, 2021 (155)
44	14KJPN Submission ignored due to conflicting rows: Row 59087132 (NC_000007.14:96999861:GC: 9572/28258) Row 59087133 (NC_000007.14:96999861:GCGCGC: 701/28258) Row 59087135 (NC_000007.14:96999861::GC 3/28258)	-	Oct 13, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 59087132 (NC_000007.14:96999861:GC: 9572/28258) Row 59087133 (NC_000007.14:96999861:GCGCGC: 701/28258) Row 59087135 (NC_000007.14:96999861::GC 3/28258)	-	Oct 13, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 59087132 (NC_000007.14:96999861:GC: 9572/28258) Row 59087133 (NC_000007.14:96999861:GCGCGC: 701/28258) Row 59087135 (NC_000007.14:96999861::GC 3/28258)	-	Oct 13, 2022 (156)
47	TopMed	NC_000007.14 - 96999862	Apr 26, 2021 (155)
48	ALFA	NC_000007.14 - 96999862	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)
rs56865584	May 27, 2008 (130)
rs57780669	May 13, 2013 (138)
rs147213460	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4169031791	NC_000007.14:96999861:GCGCGCGCGCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGC	(self)
ss4169031790	NC_000007.14:96999861:GCGCGCGCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGC	(self)
ss3720261719, ss4169031789	NC_000007.14:96999861:GCGCGCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
ss5184569953	NC_000007.13:96629173:GCGCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
ss3962145774, ss4169031788, ss5725250029	NC_000007.14:96999861:GCGCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
ss5184569955	NC_000007.13:96629173:GCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
ss4169031787	NC_000007.14:96999861:GCGC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
ss80872919	NC_000007.11:96273840:GC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
ss326966442	NC_000007.12:96467109:GC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
ss1536556521, ss3644244267, ss3785900123, ss3791189438, ss3796069431, ss5184569952	NC_000007.13:96629173:GC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
ss4169031786, ss5273961838, ss5470941666, ss5725250028	NC_000007.14:96999861:GC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
ss3962145773	NC_000007.14:96999865:GC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
ss3720261714	NC_000007.14:96999867:GC:	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGC	(self)
ss5184569954	NC_000007.13:96629173::GC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	(self)
593293349, ss4169031784, ss4755915790, ss5725250031	NC_000007.14:96999861::GC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	(self)
ss4169031785	NC_000007.14:96999861::GCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	(self)
11595461200	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	NC_000007.14:96999861:GCGCGCGCGCGC… NC_000007.14:96999861:GCGCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	(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 rs35152391

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

rs35152391