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rs1064793263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position51790404
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1064793263
dbSNP (classic)rs1064793263
ClinGenrs1064793263
ebirs1064793263
HLIrs1064793263
Exacrs1064793263
Gnomadrs1064793263
Varsomers1064793263
LitVarrs1064793263
Maprs1064793263
PheGenIrs1064793263
Biobankrs1064793263
1000 genomesrs1064793263
hgdprs1064793263
ensemblrs1064793263
geneviewrs1064793263
scholarrs1064793263
googlers1064793263
pharmgkbrs1064793263
gwascentralrs1064793263
openSNPrs1064793263
23andMers1064793263
SNPshotrs1064793263
SNPdbers1064793263
MSV3drs1064793263
GWAS Ctlgrs1064793263
Max Magnitude0
ClinVar
Risk rs1064793263(A;A)
Alt rs1064793263(A;A)
Reference Rs1064793263(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52184188G>A
CLNSRC
CLNACC RCV000480970.1,