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rs1064794873

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position51806399
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1064794873
dbSNP (old)rs1064794873
ClinGenrs1064794873
ebirs1064794873
HLIrs1064794873
Exacrs1064794873
Gnomadrs1064794873
Varsomers1064794873
Maprs1064794873
PheGenIrs1064794873
Biobankrs1064794873
1000 genomesrs1064794873
hgdprs1064794873
ensemblrs1064794873
gopubmedrs1064794873
geneviewrs1064794873
scholarrs1064794873
googlers1064794873
pharmgkbrs1064794873
gwascentralrs1064794873
openSNPrs1064794873
23andMers1064794873
23andMe allrs1064794873
SNPshotrs1064794873
SNPdbers1064794873
MSV3drs1064794873
GWAS Ctlgrs1064794873
Max Magnitude0
ClinVar
Risk rs1064794873(A;A)
Alt rs1064794873(A;A)
Reference Rs1064794873(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52200183G>A
CLNSRC
CLNACC RCV000485665.1,