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rs796053210

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053210(C;T)
Make rs796053210(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51762666
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053210
ebirs796053210
HLIrs796053210
Exacrs796053210
Varsomers796053210
Maprs796053210
PheGenIrs796053210
hapmaprs796053210
1000 genomesrs796053210
hgdprs796053210
ensemblrs796053210
gopubmedrs796053210
geneviewrs796053210
scholarrs796053210
googlers796053210
pharmgkbrs796053210
gwascentralrs796053210
openSNPrs796053210
23andMers796053210
23andMe allrs796053210
SNP Nexus

SNPshotrs796053210
SNPdbers796053210
MSV3drs796053210
GWAS Ctlgrs796053210
Max Magnitude0
ClinVar
Risk rs796053210(T;T)
Alt rs796053210(T;T)
Reference rs796053210(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52156450C>T
CLNSRC
CLNACC RCV000189266.1,