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rs1064793722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome12
Position51789419
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1064793722
dbSNP (classic)rs1064793722
ClinGenrs1064793722
ebirs1064793722
HLIrs1064793722
Exacrs1064793722
Gnomadrs1064793722
Varsomers1064793722
LitVarrs1064793722
Maprs1064793722
PheGenIrs1064793722
Biobankrs1064793722
1000 genomesrs1064793722
hgdprs1064793722
ensemblrs1064793722
geneviewrs1064793722
scholarrs1064793722
googlers1064793722
pharmgkbrs1064793722
gwascentralrs1064793722
openSNPrs1064793722
23andMers1064793722
23andMe allrs1064793722
SNPshotrs1064793722
SNPdbers1064793722
MSV3drs1064793722
GWAS Ctlgrs1064793722
Max Magnitude0
ClinVar
Risk rs1064793722(G;G)
Alt rs1064793722(G;G)
Reference Rs1064793722(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52183203A>G
CLNSRC
CLNACC RCV000479382.1,