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rs1064794730

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position165388709
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064794730
dbSNP (classic)rs1064794730
ClinGenrs1064794730
ebirs1064794730
HLIrs1064794730
Exacrs1064794730
Gnomadrs1064794730
Varsomers1064794730
LitVarrs1064794730
Maprs1064794730
PheGenIrs1064794730
Biobankrs1064794730
1000 genomesrs1064794730
hgdprs1064794730
ensemblrs1064794730
geneviewrs1064794730
scholarrs1064794730
googlers1064794730
pharmgkbrs1064794730
gwascentralrs1064794730
openSNPrs1064794730
23andMers1064794730
23andMe allrs1064794730
SNPshotrs1064794730
SNPdbers1064794730
MSV3drs1064794730
GWAS Ctlgrs1064794730
Max Magnitude0
ClinVar
Risk rs1064794730(T;T)
Alt rs1064794730(T;T)
Reference Rs1064794730(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245219C>T
CLNSRC
CLNACC RCV000479221.1,