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rs796053222

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053222(C;C)
Make rs796053222(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51806375
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053222
ebirs796053222
HLIrs796053222
Exacrs796053222
Varsomers796053222
Maprs796053222
PheGenIrs796053222
hapmaprs796053222
1000 genomesrs796053222
hgdprs796053222
ensemblrs796053222
gopubmedrs796053222
geneviewrs796053222
scholarrs796053222
googlers796053222
pharmgkbrs796053222
gwascentralrs796053222
openSNPrs796053222
23andMers796053222
23andMe allrs796053222
SNP Nexus

SNPshotrs796053222
SNPdbers796053222
MSV3drs796053222
GWAS Ctlgrs796053222
Max Magnitude0
ClinVar
Risk rs796053222(C;C)
Alt rs796053222(C;C)
Reference rs796053222(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52200159T>C
CLNSRC
CLNACC RCV000189283.1,