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rs796053233

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053233(A;A)
Make rs796053233(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51687219
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053233
ebirs796053233
HLIrs796053233
Exacrs796053233
Varsomers796053233
Maprs796053233
PheGenIrs796053233
hapmaprs796053233
1000 genomesrs796053233
hgdprs796053233
ensemblrs796053233
gopubmedrs796053233
geneviewrs796053233
scholarrs796053233
googlers796053233
pharmgkbrs796053233
gwascentralrs796053233
openSNPrs796053233
23andMers796053233
23andMe allrs796053233
SNP Nexus

SNPshotrs796053233
SNPdbers796053233
MSV3drs796053233
GWAS Ctlgrs796053233
Max Magnitude0
ClinVar
Risk rs796053233(A;A)
Alt rs796053233(A;A)
Reference rs796053233(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52081003C>A
CLNSRC
CLNACC RCV000189298.1,