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rs796053113

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053113(G;T)
Make rs796053113(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165342470
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053113
ebirs796053113
HLIrs796053113
Exacrs796053113
Varsomers796053113
Maprs796053113
PheGenIrs796053113
hapmaprs796053113
1000 genomesrs796053113
hgdprs796053113
ensemblrs796053113
gopubmedrs796053113
geneviewrs796053113
scholarrs796053113
googlers796053113
pharmgkbrs796053113
gwascentralrs796053113
openSNPrs796053113
23andMers796053113
23andMe allrs796053113
SNP Nexus

SNPshotrs796053113
SNPdbers796053113
MSV3drs796053113
GWAS Ctlgrs796053113
Max Magnitude0
ClinVar
Risk rs796053113(T;T)
Alt rs796053113(T;T)
Reference rs796053113(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166198980G>T
CLNSRC
CLNACC RCV000189115.1,