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rs1085308013

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome12
Position51699665
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1085308013
dbSNP (classic)rs1085308013
ClinGenrs1085308013
ebirs1085308013
HLIrs1085308013
Exacrs1085308013
Gnomadrs1085308013
Varsomers1085308013
LitVarrs1085308013
Maprs1085308013
PheGenIrs1085308013
Biobankrs1085308013
1000 genomesrs1085308013
hgdprs1085308013
ensemblrs1085308013
geneviewrs1085308013
scholarrs1085308013
googlers1085308013
pharmgkbrs1085308013
gwascentralrs1085308013
openSNPrs1085308013
23andMers1085308013
23andMe allrs1085308013
SNPshotrs1085308013
SNPdbers1085308013
MSV3drs1085308013
GWAS Ctlgrs1085308013
Max Magnitude0
ClinVar
Risk rs1085308013(C;C)
Alt rs1085308013(C;C)
Reference Rs1085308013(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52093449A>C
CLNSRC
CLNACC RCV000489449.1,