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rs1064795735

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position166037993
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064795735
dbSNP (old)rs1064795735
ClinGenrs1064795735
ebirs1064795735
HLIrs1064795735
Exacrs1064795735
Gnomadrs1064795735
Varsomers1064795735
LitVarrs1064795735
Maprs1064795735
PheGenIrs1064795735
Biobankrs1064795735
1000 genomesrs1064795735
hgdprs1064795735
ensemblrs1064795735
gopubmedrs1064795735
geneviewrs1064795735
scholarrs1064795735
googlers1064795735
pharmgkbrs1064795735
gwascentralrs1064795735
openSNPrs1064795735
23andMers1064795735
23andMe allrs1064795735
SNPshotrs1064795735
SNPdbers1064795735
MSV3drs1064795735
GWAS Ctlgrs1064795735
Max Magnitude0
ClinVar
Risk rs1064795735(G;G)
Alt rs1064795735(G;G)
Reference Rs1064795735(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894503T>C
CLNSRC
CLNACC RCV000487225.1,