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rs796053132

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053132(A;A)
Make rs796053132(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165374709
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053132
ebirs796053132
HLIrs796053132
Exacrs796053132
Varsomers796053132
Maprs796053132
PheGenIrs796053132
hapmaprs796053132
1000 genomesrs796053132
hgdprs796053132
ensemblrs796053132
gopubmedrs796053132
geneviewrs796053132
scholarrs796053132
googlers796053132
pharmgkbrs796053132
gwascentralrs796053132
openSNPrs796053132
23andMers796053132
23andMe allrs796053132
SNP Nexus

SNPshotrs796053132
SNPdbers796053132
MSV3drs796053132
GWAS Ctlgrs796053132
Max Magnitude0
ClinVar
Risk rs796053132(A;A)
Alt rs796053132(A;A)
Reference rs796053132(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231219G>A
CLNSRC
CLNACC RCV000189145.2,