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rs796053126

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053126(A;A)
Make rs796053126(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165354267
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053126
ebirs796053126
HLIrs796053126
Exacrs796053126
Varsomers796053126
Maprs796053126
PheGenIrs796053126
hapmaprs796053126
1000 genomesrs796053126
hgdprs796053126
ensemblrs796053126
gopubmedrs796053126
geneviewrs796053126
scholarrs796053126
googlers796053126
pharmgkbrs796053126
gwascentralrs796053126
openSNPrs796053126
23andMers796053126
23andMe allrs796053126
SNP Nexus

SNPshotrs796053126
SNPdbers796053126
MSV3drs796053126
GWAS Ctlgrs796053126
Max Magnitude0
ClinVar
Risk rs796053126(A;A)
Alt rs796053126(A;A)
Reference rs796053126(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166210777G>A
CLNSRC
CLNACC RCV000189130.2,