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rs1064795159

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position165314029
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064795159
dbSNP (old)rs1064795159
ClinGenrs1064795159
ebirs1064795159
HLIrs1064795159
Exacrs1064795159
Gnomadrs1064795159
Varsomers1064795159
Maprs1064795159
PheGenIrs1064795159
Biobankrs1064795159
1000 genomesrs1064795159
hgdprs1064795159
ensemblrs1064795159
gopubmedrs1064795159
geneviewrs1064795159
scholarrs1064795159
googlers1064795159
pharmgkbrs1064795159
gwascentralrs1064795159
openSNPrs1064795159
23andMers1064795159
23andMe allrs1064795159
SNPshotrs1064795159
SNPdbers1064795159
MSV3drs1064795159
GWAS Ctlgrs1064795159
Max Magnitude0
ClinVar
Risk rs1064795159(T;T)
Alt rs1064795159(T;T)
Reference Rs1064795159(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170539C>T
CLNSRC
CLNACC RCV000478420.1,