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rs1085307898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position165380701
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1085307898
dbSNP (classic)rs1085307898
ClinGenrs1085307898
ebirs1085307898
HLIrs1085307898
Exacrs1085307898
Gnomadrs1085307898
Varsomers1085307898
LitVarrs1085307898
Maprs1085307898
PheGenIrs1085307898
Biobankrs1085307898
1000 genomesrs1085307898
hgdprs1085307898
ensemblrs1085307898
geneviewrs1085307898
scholarrs1085307898
googlers1085307898
pharmgkbrs1085307898
gwascentralrs1085307898
openSNPrs1085307898
23andMers1085307898
SNPshotrs1085307898
SNPdbers1085307898
MSV3drs1085307898
GWAS Ctlgrs1085307898
Max Magnitude0
ClinVar
Risk rs1085307898(C;C)
Alt rs1085307898(C;C)
Reference Rs1085307898(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166237211T>C
CLNSRC
CLNACC RCV000490193.1,