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rs796053121

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053121(A;A)
Make rs796053121(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344688
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053121
ebirs796053121
HLIrs796053121
Exacrs796053121
Varsomers796053121
Maprs796053121
PheGenIrs796053121
hapmaprs796053121
1000 genomesrs796053121
hgdprs796053121
ensemblrs796053121
gopubmedrs796053121
geneviewrs796053121
scholarrs796053121
googlers796053121
pharmgkbrs796053121
gwascentralrs796053121
openSNPrs796053121
23andMers796053121
23andMe allrs796053121
SNP Nexus

SNPshotrs796053121
SNPdbers796053121
MSV3drs796053121
GWAS Ctlgrs796053121
Max Magnitude0
ClinVar
Risk rs796053121(A;A)
Alt rs796053121(A;A)
Reference rs796053121(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201198G>A
CLNSRC
CLNACC RCV000189124.1,