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rs796053157

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053157(A;A)
Make rs796053157(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165388692
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053157
ebirs796053157
HLIrs796053157
Exacrs796053157
Varsomers796053157
Maprs796053157
PheGenIrs796053157
hapmaprs796053157
1000 genomesrs796053157
hgdprs796053157
ensemblrs796053157
gopubmedrs796053157
geneviewrs796053157
scholarrs796053157
googlers796053157
pharmgkbrs796053157
gwascentralrs796053157
openSNPrs796053157
23andMers796053157
23andMe allrs796053157
SNP Nexus

SNPshotrs796053157
SNPdbers796053157
MSV3drs796053157
GWAS Ctlgrs796053157
Max Magnitude0
ClinVar
Risk rs796053157(A;A)
Alt rs796053157(A;A)
Reference rs796053157(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245202G>A
CLNSRC
CLNACC RCV000189171.1,