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rs796053131

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053131(A;A)
Make rs796053131(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165374689
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053131
ebirs796053131
HLIrs796053131
Exacrs796053131
Varsomers796053131
Maprs796053131
PheGenIrs796053131
hapmaprs796053131
1000 genomesrs796053131
hgdprs796053131
ensemblrs796053131
gopubmedrs796053131
geneviewrs796053131
scholarrs796053131
googlers796053131
pharmgkbrs796053131
gwascentralrs796053131
openSNPrs796053131
23andMers796053131
23andMe allrs796053131
SNP Nexus

SNPshotrs796053131
SNPdbers796053131
MSV3drs796053131
GWAS Ctlgrs796053131
Max Magnitude0
ClinVar
Risk rs796053131(A;A)
Alt rs796053131(A;A)
Reference rs796053131(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231199T>A
CLNSRC
CLNACC RCV000189144.2,