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rs796053211

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053211(C;C)
Make rs796053211(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51765768
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053211
ebirs796053211
HLIrs796053211
Exacrs796053211
Varsomers796053211
Maprs796053211
PheGenIrs796053211
hapmaprs796053211
1000 genomesrs796053211
hgdprs796053211
ensemblrs796053211
gopubmedrs796053211
geneviewrs796053211
scholarrs796053211
googlers796053211
pharmgkbrs796053211
gwascentralrs796053211
openSNPrs796053211
23andMers796053211
23andMe allrs796053211
SNP Nexus

SNPshotrs796053211
SNPdbers796053211
MSV3drs796053211
GWAS Ctlgrs796053211
Max Magnitude0
ClinVar
Risk rs796053211(C;C)
Alt rs796053211(C;C)
Reference rs796053211(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52159552T>C
CLNSRC
CLNACC RCV000189268.1,