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rs1085307999

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position51806378
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1085307999
dbSNP (classic)rs1085307999
ClinGenrs1085307999
ebirs1085307999
HLIrs1085307999
Exacrs1085307999
Gnomadrs1085307999
Varsomers1085307999
LitVarrs1085307999
Maprs1085307999
PheGenIrs1085307999
Biobankrs1085307999
1000 genomesrs1085307999
hgdprs1085307999
ensemblrs1085307999
geneviewrs1085307999
scholarrs1085307999
googlers1085307999
pharmgkbrs1085307999
gwascentralrs1085307999
openSNPrs1085307999
23andMers1085307999
23andMe allrs1085307999
SNPshotrs1085307999
SNPdbers1085307999
MSV3drs1085307999
GWAS Ctlgrs1085307999
Max Magnitude0
ClinVar
Risk rs1085307999(A;A)
Alt rs1085307999(A;A)
Reference Rs1085307999(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52200162T>A
CLNSRC
CLNACC RCV000488921.1,