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rs1064795736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position166037923
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064795736
dbSNP (old)rs1064795736
ClinGenrs1064795736
ebirs1064795736
HLIrs1064795736
Exacrs1064795736
Gnomadrs1064795736
Varsomers1064795736
Maprs1064795736
PheGenIrs1064795736
Biobankrs1064795736
1000 genomesrs1064795736
hgdprs1064795736
ensemblrs1064795736
gopubmedrs1064795736
geneviewrs1064795736
scholarrs1064795736
googlers1064795736
pharmgkbrs1064795736
gwascentralrs1064795736
openSNPrs1064795736
23andMers1064795736
23andMe allrs1064795736
SNPshotrs1064795736
SNPdbers1064795736
MSV3drs1064795736
GWAS Ctlgrs1064795736
Max Magnitude0
ClinVar
Risk rs1064795736(A;A)
Alt rs1064795736(A;A)
Reference Rs1064795736(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894433G>T
CLNSRC
CLNACC RCV000479119.1,