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dbSNP Short Genetic Variations

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.

rs369560930

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr17:7221580 (GRCh38.p13) 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
G>A / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.000057 (15/264690, TOPMED)
A=0.000086 (12/140174, GnomAD)
A=0.00009 (4/46770, ALFA) (+ 4 more)
A=0.00008 (1/13006, GO-ESP)
A=0.0007 (3/4480, Estonian)
A=0.0003 (1/3854, ALSPAC)
A=0.0000 (0/3708, TWINSUK)
Clinical Significance
Reported in ClinVar
Gene : Consequence
ACADVL : Missense Variant
DLG4 : 2KB Upstream Variant
Publications
7 citations
Genomic View
See rs on genome
Help

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.p13 chr 17 NC_000017.11:g.7221580G>A
GRCh38.p13 chr 17 NC_000017.11:g.7221580G>T
GRCh37.p13 chr 17 NC_000017.10:g.7124899G>A
GRCh37.p13 chr 17 NC_000017.10:g.7124899G>T
DLG4 RefSeqGene NG_008391.2:g.3471C>T
DLG4 RefSeqGene NG_008391.2:g.3471C>A
ACADVL RefSeqGene NG_007975.1:g.6747G>A
ACADVL RefSeqGene NG_007975.1:g.6747G>T
Gene: DLG4, discs large MAGUK scaffold protein 4 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
DLG4 transcript variant 3 NM_001321074.1:c. N/A Upstream Transcript Variant
DLG4 transcript variant 1 NM_001365.4:c. N/A Upstream Transcript Variant
DLG4 transcript variant 2 NM_001128827.4:c. N/A N/A
DLG4 transcript variant 4 NM_001321075.3:c. N/A N/A
DLG4 transcript variant 5 NM_001321076.3:c. N/A N/A
DLG4 transcript variant 6 NM_001321077.3:c. N/A N/A
DLG4 transcript variant 8 NM_001369566.3:c. N/A N/A
DLG4 transcript variant 7 NR_135527.1:n. N/A Upstream Transcript Variant
DLG4 transcript variant X1 XM_011523699.2:c. N/A Upstream Transcript Variant
DLG4 transcript variant X2 XM_005256491.1:c. N/A N/A
DLG4 transcript variant X8 XM_011523702.1:c. N/A N/A
DLG4 transcript variant X4 XM_017024288.2:c. N/A N/A
DLG4 transcript variant X5 XM_017024289.2:c. N/A N/A
DLG4 transcript variant X3 XM_024450629.1:c. N/A N/A
DLG4 transcript variant X7 XR_934005.2:n. N/A Upstream Transcript Variant
Gene: ACADVL, acyl-CoA dehydrogenase very long chain (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ACADVL transcript variant 1 NM_000018.4:c.520G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 1 precursor NP_000009.1:p.Val174Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant 1 NM_000018.4:c.520G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 1 precursor NP_000009.1:p.Val174Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant 2 NM_001033859.3:c.454G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 2 precursor NP_001029031.1:p.Val152Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant 2 NM_001033859.3:c.454G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 2 precursor NP_001029031.1:p.Val152Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant 4 NM_001270448.2:c.292G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 4 NP_001257377.1:p.Val98Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant 4 NM_001270448.2:c.292G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 4 NP_001257377.1:p.Val98Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant 3 NM_001270447.2:c.589G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 3 NP_001257376.1:p.Val197Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant 3 NM_001270447.2:c.589G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 3 NP_001257376.1:p.Val197Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant X1 XM_006721516.3:c.520G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1 XP_006721579.2:p.Val174Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant X1 XM_006721516.3:c.520G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1 XP_006721579.2:p.Val174Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant X2 XM_024450741.1:c.520G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2 XP_024306509.1:p.Val174Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant X2 XM_024450741.1:c.520G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2 XP_024306509.1:p.Val174Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant X3 XM_011523829.2:c.520G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X3 XP_011522131.1:p.Val174Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant X3 XM_011523829.2:c.520G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X3 XP_011522131.1:p.Val174Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant X4 XM_011523830.2:c.520G>A V [GTG] > M [ATG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X4 XP_011522132.1:p.Val174Met V (Val) > M (Met) Missense Variant
ACADVL transcript variant X4 XM_011523830.2:c.520G>T V [GTG] > L [TTG] Coding Sequence Variant
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X4 XP_011522132.1:p.Val174Leu V (Val) > L (Leu) Missense Variant
ACADVL transcript variant X5 XR_934021.2:n.579G>A N/A Non Coding Transcript Variant
ACADVL transcript variant X5 XR_934021.2:n.579G>T N/A Non Coding Transcript Variant
ACADVL transcript variant X6 XR_934022.2:n.579G>A N/A Non Coding Transcript Variant
ACADVL transcript variant X6 XR_934022.2:n.579G>T N/A Non Coding Transcript Variant
ACADVL transcript variant X7 XR_934023.2:n.579G>A N/A Non Coding Transcript Variant
ACADVL transcript variant X7 XR_934023.2:n.579G>T N/A Non Coding Transcript Variant
Help

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.

Allele: A (allele ID: 98197 )
ClinVar Accession Disease Names Clinical Significance
RCV000077919.7 not provided Pathogenic-Likely-Pathogenic
RCV000179696.10 Very long chain acyl-CoA dehydrogenase deficiency Pathogenic-Likely-Pathogenic

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 46770 G=0.99991 A=0.00009
European Sub 37190 G=0.99989 A=0.00011
African Sub 3344 G=1.0000 A=0.0000
African Others Sub 114 G=1.000 A=0.000
African American Sub 3230 G=1.0000 A=0.0000
Asian Sub 112 G=1.000 A=0.000
East Asian Sub 86 G=1.00 A=0.00
Other Asian Sub 26 G=1.00 A=0.00
Latin American 1 Sub 500 G=1.000 A=0.000
Latin American 2 Sub 628 G=1.000 A=0.000
South Asian Sub 98 G=1.00 A=0.00
Other Sub 4898 G=1.0000 A=0.0000


Help

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
TopMed Global Study-wide 264690 G=0.999943 A=0.000057
gnomAD - Genomes Global Study-wide 140174 G=0.999914 A=0.000086
gnomAD - Genomes European Sub 75922 G=0.99992 A=0.00008
gnomAD - Genomes African Sub 42000 G=0.99986 A=0.00014
gnomAD - Genomes American Sub 13652 G=1.00000 A=0.00000
gnomAD - Genomes Ashkenazi Jewish Sub 3324 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3134 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2142 G=1.0000 A=0.0000
GO Exome Sequencing Project Global Study-wide 13006 G=0.99992 A=0.00008
GO Exome Sequencing Project European American Sub 8600 G=0.9999 A=0.0001
GO Exome Sequencing Project African American Sub 4406 G=1.0000 A=0.0000
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9993 A=0.0007
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9997 A=0.0003
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=1.0000 A=0.0000
Help

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 G= A T
GRCh38.p13 chr 17 NC_000017.11:g.7221580= NC_000017.11:g.7221580G>A NC_000017.11:g.7221580G>T
GRCh37.p13 chr 17 NC_000017.10:g.7124899= NC_000017.10:g.7124899G>A NC_000017.10:g.7124899G>T
DLG4 RefSeqGene NG_008391.2:g.3471= NG_008391.2:g.3471C>T NG_008391.2:g.3471C>A
ACADVL RefSeqGene NG_007975.1:g.6747= NG_007975.1:g.6747G>A NG_007975.1:g.6747G>T
ACADVL transcript variant 1 NM_000018.4:c.520= NM_000018.4:c.520G>A NM_000018.4:c.520G>T
ACADVL transcript variant 1 NM_000018.3:c.520= NM_000018.3:c.520G>A NM_000018.3:c.520G>T
ACADVL transcript variant 2 NM_001033859.3:c.454= NM_001033859.3:c.454G>A NM_001033859.3:c.454G>T
ACADVL transcript variant 2 NM_001033859.2:c.454= NM_001033859.2:c.454G>A NM_001033859.2:c.454G>T
ACADVL transcript variant 4 NM_001270448.2:c.292= NM_001270448.2:c.292G>A NM_001270448.2:c.292G>T
ACADVL transcript variant 4 NM_001270448.1:c.292= NM_001270448.1:c.292G>A NM_001270448.1:c.292G>T
ACADVL transcript variant 3 NM_001270447.2:c.589= NM_001270447.2:c.589G>A NM_001270447.2:c.589G>T
ACADVL transcript variant 3 NM_001270447.1:c.589= NM_001270447.1:c.589G>A NM_001270447.1:c.589G>T
ACADVL transcript variant X1 XM_006721516.3:c.520= XM_006721516.3:c.520G>A XM_006721516.3:c.520G>T
ACADVL transcript variant X5 XR_934021.2:n.579= XR_934021.2:n.579G>A XR_934021.2:n.579G>T
ACADVL transcript variant X7 XR_934023.2:n.579= XR_934023.2:n.579G>A XR_934023.2:n.579G>T
ACADVL transcript variant X3 XM_011523829.2:c.520= XM_011523829.2:c.520G>A XM_011523829.2:c.520G>T
ACADVL transcript variant X6 XR_934022.2:n.579= XR_934022.2:n.579G>A XR_934022.2:n.579G>T
ACADVL transcript variant X4 XM_011523830.2:c.520= XM_011523830.2:c.520G>A XM_011523830.2:c.520G>T
ACADVL transcript variant X2 XM_024450741.1:c.520= XM_024450741.1:c.520G>A XM_024450741.1:c.520G>T
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 1 precursor NP_000009.1:p.Val174= NP_000009.1:p.Val174Met NP_000009.1:p.Val174Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 2 precursor NP_001029031.1:p.Val152= NP_001029031.1:p.Val152Met NP_001029031.1:p.Val152Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 4 NP_001257377.1:p.Val98= NP_001257377.1:p.Val98Met NP_001257377.1:p.Val98Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform 3 NP_001257376.1:p.Val197= NP_001257376.1:p.Val197Met NP_001257376.1:p.Val197Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1 XP_006721579.2:p.Val174= XP_006721579.2:p.Val174Met XP_006721579.2:p.Val174Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X3 XP_011522131.1:p.Val174= XP_011522131.1:p.Val174Met XP_011522131.1:p.Val174Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X4 XP_011522132.1:p.Val174= XP_011522132.1:p.Val174Met XP_011522132.1:p.Val174Leu
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2 XP_024306509.1:p.Val174= XP_024306509.1:p.Val174Met XP_024306509.1:p.Val174Leu
Help

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#.

23 SubSNP, 11 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 NHLBI-ESP ss713354515 Apr 25, 2013 (138)
2 EGL ss947846746 Jan 23, 2014 (138)
3 EVA_UK10K_ALSPAC ss1635234090 Apr 01, 2015 (144)
4 EVA_UK10K_TWINSUK ss1678228123 Apr 01, 2015 (144)
5 EVA_EXAC ss1692563586 Apr 01, 2015 (144)
6 EVA_EXAC ss1692563587 Apr 01, 2015 (144)
7 HUMAN_LONGEVITY ss2215291724 Dec 20, 2016 (150)
8 TOPMED ss2380138911 Dec 20, 2016 (150)
9 GNOMAD ss2742385590 Nov 08, 2017 (151)
10 GNOMAD ss2749672639 Nov 08, 2017 (151)
11 GNOMAD ss2947395418 Nov 08, 2017 (151)
12 AFFY ss2985084257 Nov 08, 2017 (151)
13 SWEGEN ss3015151821 Nov 08, 2017 (151)
14 ILLUMINA ss3021751262 Nov 08, 2017 (151)
15 ILLUMINA ss3021751263 Nov 08, 2017 (151)
16 TOPMED ss3256594143 Nov 08, 2017 (151)
17 ILLUMINA ss3652164041 Oct 12, 2018 (152)
18 ILLUMINA ss3652164042 Oct 12, 2018 (152)
19 ILLUMINA ss3653856530 Oct 12, 2018 (152)
20 EGCUT_WGS ss3682117385 Jul 13, 2019 (153)
21 ILLUMINA ss3725599163 Jul 13, 2019 (153)
22 EVA ss3825070553 Apr 27, 2020 (154)
23 TOPMED ss5028550275 Apr 27, 2021 (155)
24 The Avon Longitudinal Study of Parents and Children NC_000017.10 - 7124899 Oct 12, 2018 (152)
25 Genetic variation in the Estonian population NC_000017.10 - 7124899 Oct 12, 2018 (152)
26 ExAC

Submission ignored due to conflicting rows:
Row 2990133 (NC_000017.10:7124898:G:G 121300/121306, NC_000017.10:7124898:G:A 6/121306)
Row 2990134 (NC_000017.10:7124898:G:G 121305/121306, NC_000017.10:7124898:G:T 1/121306)

- Oct 12, 2018 (152)
27 ExAC

Submission ignored due to conflicting rows:
Row 2990133 (NC_000017.10:7124898:G:G 121300/121306, NC_000017.10:7124898:G:A 6/121306)
Row 2990134 (NC_000017.10:7124898:G:G 121305/121306, NC_000017.10:7124898:G:T 1/121306)

- Oct 12, 2018 (152)
28 gnomAD - Genomes NC_000017.11 - 7221580 Apr 27, 2021 (155)
29 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 11683006 (NC_000017.10:7124898:G:G 251463/251474, NC_000017.10:7124898:G:A 11/251474)
Row 11683007 (NC_000017.10:7124898:G:G 251473/251474, NC_000017.10:7124898:G:T 1/251474)

- Jul 13, 2019 (153)
30 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 11683006 (NC_000017.10:7124898:G:G 251463/251474, NC_000017.10:7124898:G:A 11/251474)
Row 11683007 (NC_000017.10:7124898:G:G 251473/251474, NC_000017.10:7124898:G:T 1/251474)

- Jul 13, 2019 (153)
31 GO Exome Sequencing Project NC_000017.10 - 7124899 Oct 12, 2018 (152)
32 TopMed NC_000017.11 - 7221580 Apr 27, 2021 (155)
33 UK 10K study - Twins NC_000017.10 - 7124899 Oct 12, 2018 (152)
34 ALFA NC_000017.11 - 7221580 Apr 27, 2021 (155)
35 ClinVar RCV000077919.7 Apr 27, 2020 (154)
36 ClinVar RCV000179696.10 Apr 27, 2021 (155)
Help

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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
39384212, 27855633, 1527682, 39384212, ss713354515, ss1635234090, ss1678228123, ss1692563586, ss2380138911, ss2742385590, ss2749672639, ss2947395418, ss2985084257, ss3015151821, ss3021751262, ss3652164041, ss3653856530, ss3682117385, ss3825070553 NC_000017.10:7124898:G:A NC_000017.11:7221579:G:A (self)
RCV000077919.7, RCV000179696.10, 500715961, 152330364, 244095937, 4066345554, ss947846746, ss2215291724, ss3256594143, ss3725599163, ss5028550275 NC_000017.11:7221579:G:A NC_000017.11:7221579:G:A (self)
ss1692563587, ss2742385590, ss3021751263, ss3652164042 NC_000017.10:7124898:G:T NC_000017.11:7221579:G:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

7 citations for rs369560930
PMID Title Author Year Journal
9973285 Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency. Andresen BS et al. 1999 American journal of human genetics
17999356 Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy. Gobin-Limballe S et al. 2007 American journal of human genetics
18670371 Development of a new enzymatic diagnosis method for very-long-chain Acyl-CoA dehydrogenase deficiency by detecting 2-hexadecenoyl-CoA production and its application in tandem mass spectrometry-based selective screening and newborn screening in Japan. Tajima G et al. 2008 Pediatric research
20060901 Compared effects of missense mutations in Very-Long-Chain Acyl-CoA Dehydrogenase deficiency: Combined analysis by structural, functional and pharmacological approaches. Gobin-Limballe S et al. 2010 Biochimica et biophysica acta
23430950 Successful weight loss in two adult patients diagnosed with late-onset long-chain Fatty Acid oxidation defect. Zweers H et al. 2012 JIMD reports
23757202 Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data. Bean LJ et al. 2013 Human mutation
26881790 Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency. Diekman EF et al. 2016 PloS one
Help

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.

Software version is: 2.0.1.post596+ae089ad