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rs796053062

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053062(-;-)
Make rs796053062(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166043893
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053062
ebirs796053062
HLIrs796053062
Exacrs796053062
Varsomers796053062
Maprs796053062
PheGenIrs796053062
hapmaprs796053062
1000 genomesrs796053062
hgdprs796053062
ensemblrs796053062
gopubmedrs796053062
geneviewrs796053062
scholarrs796053062
googlers796053062
pharmgkbrs796053062
gwascentralrs796053062
openSNPrs796053062
23andMers796053062
23andMe allrs796053062
SNP Nexus

SNPshotrs796053062
SNPdbers796053062
MSV3drs796053062
GWAS Ctlgrs796053062
Max Magnitude0
ClinVar
Risk rs796053062(;)
Alt rs796053062(;)
Reference rs796053062(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166900403delA
CLNSRC
CLNACC RCV000189042.1,