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rs1064795085

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position38599020
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1064795085
dbSNP (classic)rs1064795085
ClinGenrs1064795085
ebirs1064795085
HLIrs1064795085
Exacrs1064795085
Gnomadrs1064795085
Varsomers1064795085
LitVarrs1064795085
Maprs1064795085
PheGenIrs1064795085
Biobankrs1064795085
1000 genomesrs1064795085
hgdprs1064795085
ensemblrs1064795085
geneviewrs1064795085
scholarrs1064795085
googlers1064795085
pharmgkbrs1064795085
gwascentralrs1064795085
openSNPrs1064795085
23andMers1064795085
SNPshotrs1064795085
SNPdbers1064795085
MSV3drs1064795085
GWAS Ctlgrs1064795085
Max Magnitude0
ClinVar
Risk rs1064795085(T;T)
Alt rs1064795085(T;T)
Reference Rs1064795085(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38640511G>A
CLNSRC
CLNACC RCV000482074.1,