Have questions? Visit https://www.reddit.com/r/SNPedia

rs761117662

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761117662(C;G)
Make rs761117662(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38606016
GeneSCN5A
is asnp
is mentioned by
dbSNPrs761117662
ebirs761117662
HLIrs761117662
Exacrs761117662
Varsomers761117662
Maprs761117662
PheGenIrs761117662
hapmaprs761117662
1000 genomesrs761117662
hgdprs761117662
ensemblrs761117662
gopubmedrs761117662
geneviewrs761117662
scholarrs761117662
googlers761117662
pharmgkbrs761117662
gwascentralrs761117662
openSNPrs761117662
23andMers761117662
23andMe allrs761117662
SNP Nexus

SNPshotrs761117662
SNPdbers761117662
MSV3drs761117662
GWAS Ctlgrs761117662
Max Magnitude0
ClinVar
Risk rs761117662(T;T)
Alt rs761117662(T;T)
Reference rs761117662(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38647507C>T
CLNSRC
CLNACC RCV000182966.2,