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rs1064797266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position166058687
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064797266
dbSNP (classic)rs1064797266
ClinGenrs1064797266
ebirs1064797266
HLIrs1064797266
Exacrs1064797266
Gnomadrs1064797266
Varsomers1064797266
LitVarrs1064797266
Maprs1064797266
PheGenIrs1064797266
Biobankrs1064797266
1000 genomesrs1064797266
hgdprs1064797266
ensemblrs1064797266
geneviewrs1064797266
scholarrs1064797266
googlers1064797266
pharmgkbrs1064797266
gwascentralrs1064797266
openSNPrs1064797266
23andMers1064797266
23andMe allrs1064797266
SNPshotrs1064797266
SNPdbers1064797266
MSV3drs1064797266
GWAS Ctlgrs1064797266
Max Magnitude0
ClinVar
Risk rs1064797266(-;-)
Alt rs1064797266(-;-)
Reference Rs1064797266(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915197delG
CLNSRC
CLNACC RCV000487842.1,