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

rs796053184

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053184(A;A)
Make rs796053184(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165314037
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053184
ebirs796053184
HLIrs796053184
Exacrs796053184
Varsomers796053184
Maprs796053184
PheGenIrs796053184
hapmaprs796053184
1000 genomesrs796053184
hgdprs796053184
ensemblrs796053184
gopubmedrs796053184
geneviewrs796053184
scholarrs796053184
googlers796053184
pharmgkbrs796053184
gwascentralrs796053184
openSNPrs796053184
23andMers796053184
23andMe allrs796053184
SNP Nexus

SNPshotrs796053184
SNPdbers796053184
MSV3drs796053184
GWAS Ctlgrs796053184
Max Magnitude0
ClinVar
Risk rs796053184(A;A)
Alt rs796053184(A;A)
Reference rs796053184(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170547G>A
CLNSRC
CLNACC RCV000189211.1,