Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position166054731
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064793315
dbSNP (classic)rs1064793315
ClinGenrs1064793315
ebirs1064793315
HLIrs1064793315
Exacrs1064793315
Gnomadrs1064793315
Varsomers1064793315
LitVarrs1064793315
Maprs1064793315
PheGenIrs1064793315
Biobankrs1064793315
1000 genomesrs1064793315
hgdprs1064793315
ensemblrs1064793315
geneviewrs1064793315
scholarrs1064793315
googlers1064793315
pharmgkbrs1064793315
gwascentralrs1064793315
openSNPrs1064793315
23andMers1064793315
23andMe allrs1064793315
SNPshotrs1064793315
SNPdbers1064793315
MSV3drs1064793315
GWAS Ctlgrs1064793315
Max Magnitude0
ClinVar
Risk rs1064793315(C;C)
Alt rs1064793315(C;C)
Reference Rs1064793315(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166911241A>G
CLNSRC
CLNACC RCV000481626.1,