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rs1064794630

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position165992000
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064794630
dbSNP (old)rs1064794630
ClinGenrs1064794630
ebirs1064794630
HLIrs1064794630
Exacrs1064794630
Gnomadrs1064794630
Varsomers1064794630
Maprs1064794630
PheGenIrs1064794630
Biobankrs1064794630
1000 genomesrs1064794630
hgdprs1064794630
ensemblrs1064794630
gopubmedrs1064794630
geneviewrs1064794630
scholarrs1064794630
googlers1064794630
pharmgkbrs1064794630
gwascentralrs1064794630
openSNPrs1064794630
23andMers1064794630
23andMe allrs1064794630
SNPshotrs1064794630
SNPdbers1064794630
MSV3drs1064794630
GWAS Ctlgrs1064794630
Max Magnitude0
ClinVar
Risk rs1064794630(T;T)
Alt rs1064794630(T;T)
Reference Rs1064794630(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848510G>A
CLNSRC
CLNACC RCV000479372.1,