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rs1064794243

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome17
Position63941169
GeneSCN4A
is asnp
is mentioned by
dbSNPrs1064794243
dbSNP (old)rs1064794243
ClinGenrs1064794243
ebirs1064794243
HLIrs1064794243
Exacrs1064794243
Gnomadrs1064794243
Varsomers1064794243
Maprs1064794243
PheGenIrs1064794243
Biobankrs1064794243
1000 genomesrs1064794243
hgdprs1064794243
ensemblrs1064794243
gopubmedrs1064794243
geneviewrs1064794243
scholarrs1064794243
googlers1064794243
pharmgkbrs1064794243
gwascentralrs1064794243
openSNPrs1064794243
23andMers1064794243
23andMe allrs1064794243
SNPshotrs1064794243
SNPdbers1064794243
MSV3drs1064794243
GWAS Ctlgrs1064794243
Max Magnitude0
ClinVar
Risk rs1064794243(A;A)
Alt rs1064794243(A;A)
Reference Rs1064794243(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN4A
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.62018529A>T
CLNSRC
CLNACC RCV000484046.1,