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rs796053191

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053191(C;C)
Make rs796053191(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165331486
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053191
ebirs796053191
HLIrs796053191
Exacrs796053191
Varsomers796053191
Maprs796053191
PheGenIrs796053191
hapmaprs796053191
1000 genomesrs796053191
hgdprs796053191
ensemblrs796053191
gopubmedrs796053191
geneviewrs796053191
scholarrs796053191
googlers796053191
pharmgkbrs796053191
gwascentralrs796053191
openSNPrs796053191
23andMers796053191
23andMe allrs796053191
SNP Nexus

SNPshotrs796053191
SNPdbers796053191
MSV3drs796053191
GWAS Ctlgrs796053191
Max Magnitude0
ClinVar
Risk rs796053191(C;C)
Alt rs796053191(C;C)
Reference rs796053191(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166187996T>C
CLNSRC
CLNACC RCV000189229.1,