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rs796052985

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052985(C;T)
Make rs796052985(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166037940
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052985
ebirs796052985
HLIrs796052985
Exacrs796052985
Varsomers796052985
Maprs796052985
PheGenIrs796052985
hapmaprs796052985
1000 genomesrs796052985
hgdprs796052985
ensemblrs796052985
gopubmedrs796052985
geneviewrs796052985
scholarrs796052985
googlers796052985
pharmgkbrs796052985
gwascentralrs796052985
openSNPrs796052985
23andMers796052985
23andMe allrs796052985
SNP Nexus

SNPshotrs796052985
SNPdbers796052985
MSV3drs796052985
GWAS Ctlgrs796052985
Max Magnitude0
ClinVar
Risk rs796052985(T;T)
Alt rs796052985(T;T)
Reference rs796052985(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894450G>A
CLNSRC
CLNACC RCV000188896.1,