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rs796053197

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053197(C;T)
Make rs796053197(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344801
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053197
ebirs796053197
HLIrs796053197
Exacrs796053197
Varsomers796053197
Maprs796053197
PheGenIrs796053197
hapmaprs796053197
1000 genomesrs796053197
hgdprs796053197
ensemblrs796053197
gopubmedrs796053197
geneviewrs796053197
scholarrs796053197
googlers796053197
pharmgkbrs796053197
gwascentralrs796053197
openSNPrs796053197
23andMers796053197
23andMe allrs796053197
SNP Nexus

SNPshotrs796053197
SNPdbers796053197
MSV3drs796053197
GWAS Ctlgrs796053197
Max Magnitude0
ClinVar
Risk rs796053197(T;T)
Alt rs796053197(T;T)
Reference rs796053197(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201311C>T
CLNSRC
CLNACC RCV000189235.2,