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rs1064795620

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position166045045
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064795620
dbSNP (old)rs1064795620
ClinGenrs1064795620
ebirs1064795620
HLIrs1064795620
Exacrs1064795620
Gnomadrs1064795620
Varsomers1064795620
Maprs1064795620
PheGenIrs1064795620
Biobankrs1064795620
1000 genomesrs1064795620
hgdprs1064795620
ensemblrs1064795620
gopubmedrs1064795620
geneviewrs1064795620
scholarrs1064795620
googlers1064795620
pharmgkbrs1064795620
gwascentralrs1064795620
openSNPrs1064795620
23andMers1064795620
23andMe allrs1064795620
SNPshotrs1064795620
SNPdbers1064795620
MSV3drs1064795620
GWAS Ctlgrs1064795620
Max Magnitude0
ClinVar
Risk rs1064795620(T;T)
Alt rs1064795620(T;T)
Reference Rs1064795620(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166901555G>A
CLNSRC
CLNACC RCV000482122.1,