Have questions? Visit https://www.reddit.com/r/SNPedia

rs796053173

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053173(A;G)
Make rs796053173(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165310476
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053173
ebirs796053173
HLIrs796053173
Exacrs796053173
Varsomers796053173
Maprs796053173
PheGenIrs796053173
hapmaprs796053173
1000 genomesrs796053173
hgdprs796053173
ensemblrs796053173
gopubmedrs796053173
geneviewrs796053173
scholarrs796053173
googlers796053173
pharmgkbrs796053173
gwascentralrs796053173
openSNPrs796053173
23andMers796053173
23andMe allrs796053173
SNP Nexus

SNPshotrs796053173
SNPdbers796053173
MSV3drs796053173
GWAS Ctlgrs796053173
Max Magnitude0
ClinVar
Risk rs796053173(G;G)
Alt rs796053173(G;G)
Reference rs796053173(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166986A>G
CLNSRC
CLNACC RCV000189197.1,