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rs796053118

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053118(C;C)
Make rs796053118(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344649
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053118
ebirs796053118
HLIrs796053118
Exacrs796053118
Varsomers796053118
Maprs796053118
PheGenIrs796053118
hapmaprs796053118
1000 genomesrs796053118
hgdprs796053118
ensemblrs796053118
gopubmedrs796053118
geneviewrs796053118
scholarrs796053118
googlers796053118
pharmgkbrs796053118
gwascentralrs796053118
openSNPrs796053118
23andMers796053118
23andMe allrs796053118
SNP Nexus

SNPshotrs796053118
SNPdbers796053118
MSV3drs796053118
GWAS Ctlgrs796053118
Max Magnitude0
ClinVar
Risk rs796053118(C;C)
Alt rs796053118(C;C)
Reference rs796053118(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201159T>C
CLNSRC
CLNACC RCV000189120.2,