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rs1085307940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position51762657
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1085307940
dbSNP (classic)rs1085307940
ClinGenrs1085307940
ebirs1085307940
HLIrs1085307940
Exacrs1085307940
Gnomadrs1085307940
Varsomers1085307940
LitVarrs1085307940
Maprs1085307940
PheGenIrs1085307940
Biobankrs1085307940
1000 genomesrs1085307940
hgdprs1085307940
ensemblrs1085307940
geneviewrs1085307940
scholarrs1085307940
googlers1085307940
pharmgkbrs1085307940
gwascentralrs1085307940
openSNPrs1085307940
23andMers1085307940
23andMe allrs1085307940
SNPshotrs1085307940
SNPdbers1085307940
MSV3drs1085307940
GWAS Ctlgrs1085307940
Max Magnitude0
ClinVar
Risk rs1085307940(A;A)
Alt rs1085307940(A;A)
Reference Rs1085307940(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52156441T>A
CLNSRC
CLNACC RCV000489752.1,