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rs796053133

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053133(G;G)
Make rs796053133(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165374725
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053133
ebirs796053133
HLIrs796053133
Exacrs796053133
Varsomers796053133
Maprs796053133
PheGenIrs796053133
hapmaprs796053133
1000 genomesrs796053133
hgdprs796053133
ensemblrs796053133
gopubmedrs796053133
geneviewrs796053133
scholarrs796053133
googlers796053133
pharmgkbrs796053133
gwascentralrs796053133
openSNPrs796053133
23andMers796053133
23andMe allrs796053133
SNP Nexus

SNPshotrs796053133
SNPdbers796053133
MSV3drs796053133
GWAS Ctlgrs796053133
Max Magnitude0
ClinVar
Risk rs796053133(G;G)
Alt rs796053133(G;G)
Reference rs796053133(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231235T>G
CLNSRC
CLNACC RCV000189146.2,