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rs796052988

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052988(G;T)
Make rs796052988(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166037916
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052988
ebirs796052988
HLIrs796052988
Exacrs796052988
Varsomers796052988
Maprs796052988
PheGenIrs796052988
hapmaprs796052988
1000 genomesrs796052988
hgdprs796052988
ensemblrs796052988
gopubmedrs796052988
geneviewrs796052988
scholarrs796052988
googlers796052988
pharmgkbrs796052988
gwascentralrs796052988
openSNPrs796052988
23andMers796052988
23andMe allrs796052988
SNP Nexus

SNPshotrs796052988
SNPdbers796052988
MSV3drs796052988
GWAS Ctlgrs796052988
Max Magnitude0
ClinVar
Risk rs796052988(T;T)
Alt rs796052988(T;T)
Reference rs796052988(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894426C>A
CLNSRC
CLNACC RCV000188900.2,