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rs1064797019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position166038078
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064797019
dbSNP (old)rs1064797019
ClinGenrs1064797019
ebirs1064797019
HLIrs1064797019
Exacrs1064797019
Gnomadrs1064797019
Varsomers1064797019
LitVarrs1064797019
Maprs1064797019
PheGenIrs1064797019
Biobankrs1064797019
1000 genomesrs1064797019
hgdprs1064797019
ensemblrs1064797019
gopubmedrs1064797019
geneviewrs1064797019
scholarrs1064797019
googlers1064797019
pharmgkbrs1064797019
gwascentralrs1064797019
openSNPrs1064797019
23andMers1064797019
23andMe allrs1064797019
SNPshotrs1064797019
SNPdbers1064797019
MSV3drs1064797019
GWAS Ctlgrs1064797019
Max Magnitude0
ClinVar
Risk rs1064797019(T;T)
Alt rs1064797019(T;T)
Reference Rs1064797019(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894588T>A
CLNSRC
CLNACC RCV000484204.1,