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rs796053116

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053116(A;A)
Make rs796053116(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344634
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053116
ebirs796053116
HLIrs796053116
Exacrs796053116
Varsomers796053116
Maprs796053116
PheGenIrs796053116
hapmaprs796053116
1000 genomesrs796053116
hgdprs796053116
ensemblrs796053116
gopubmedrs796053116
geneviewrs796053116
scholarrs796053116
googlers796053116
pharmgkbrs796053116
gwascentralrs796053116
openSNPrs796053116
23andMers796053116
23andMe allrs796053116
SNP Nexus

SNPshotrs796053116
SNPdbers796053116
MSV3drs796053116
GWAS Ctlgrs796053116
Max Magnitude0
ClinVar
Risk rs796053116(A;A)
Alt rs796053116(A;A)
Reference rs796053116(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201144T>A
CLNSRC
CLNACC RCV000189118.1,