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rs796053172

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053172(C;G)
Make rs796053172(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165310415
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053172
ebirs796053172
HLIrs796053172
Exacrs796053172
Varsomers796053172
Maprs796053172
PheGenIrs796053172
hapmaprs796053172
1000 genomesrs796053172
hgdprs796053172
ensemblrs796053172
gopubmedrs796053172
geneviewrs796053172
scholarrs796053172
googlers796053172
pharmgkbrs796053172
gwascentralrs796053172
openSNPrs796053172
23andMers796053172
23andMe allrs796053172
SNP Nexus

SNPshotrs796053172
SNPdbers796053172
MSV3drs796053172
GWAS Ctlgrs796053172
Max Magnitude0
ClinVar
Risk rs796053172(G;G)
Alt rs796053172(G;G)
Reference rs796053172(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166925C>G
CLNSRC
CLNACC RCV000189194.1,