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rs796053209

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053209(A;G)
Make rs796053209(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51702879
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053209
ebirs796053209
HLIrs796053209
Exacrs796053209
Varsomers796053209
Maprs796053209
PheGenIrs796053209
hapmaprs796053209
1000 genomesrs796053209
hgdprs796053209
ensemblrs796053209
gopubmedrs796053209
geneviewrs796053209
scholarrs796053209
googlers796053209
pharmgkbrs796053209
gwascentralrs796053209
openSNPrs796053209
23andMers796053209
23andMe allrs796053209
SNP Nexus

SNPshotrs796053209
SNPdbers796053209
MSV3drs796053209
GWAS Ctlgrs796053209
Max Magnitude0
ClinVar
Risk rs796053209(G;G)
Alt rs796053209(G;G)
Reference rs796053209(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52096663A>G
CLNSRC
CLNACC RCV000189260.2,