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rs1064795018

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position165310400
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064795018
dbSNP (old)rs1064795018
ClinGenrs1064795018
ebirs1064795018
HLIrs1064795018
Exacrs1064795018
Gnomadrs1064795018
Varsomers1064795018
LitVarrs1064795018
Maprs1064795018
PheGenIrs1064795018
Biobankrs1064795018
1000 genomesrs1064795018
hgdprs1064795018
ensemblrs1064795018
gopubmedrs1064795018
geneviewrs1064795018
scholarrs1064795018
googlers1064795018
pharmgkbrs1064795018
gwascentralrs1064795018
openSNPrs1064795018
23andMers1064795018
23andMe allrs1064795018
SNPshotrs1064795018
SNPdbers1064795018
MSV3drs1064795018
GWAS Ctlgrs1064795018
Max Magnitude0
ClinVar
Risk rs1064795018(A;A)
Alt rs1064795018(A;A)
Reference Rs1064795018(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166910C>A
CLNSRC
CLNACC RCV000486566.1,