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

rs796053162

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053162(A;A)
Make rs796053162(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165389123
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053162
ebirs796053162
HLIrs796053162
Exacrs796053162
Varsomers796053162
Maprs796053162
PheGenIrs796053162
hapmaprs796053162
1000 genomesrs796053162
hgdprs796053162
ensemblrs796053162
gopubmedrs796053162
geneviewrs796053162
scholarrs796053162
googlers796053162
pharmgkbrs796053162
gwascentralrs796053162
openSNPrs796053162
23andMers796053162
23andMe allrs796053162
SNP Nexus

SNPshotrs796053162
SNPdbers796053162
MSV3drs796053162
GWAS Ctlgrs796053162
Max Magnitude0
ClinVar
Risk rs796053162(A;A)
Alt rs796053162(A;A)
Reference rs796053162(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245633G>A
CLNSRC
CLNACC RCV000189176.1,