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rs796053227

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053227(C;T)
Make rs796053227(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51807041
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053227
ebirs796053227
HLIrs796053227
Exacrs796053227
Varsomers796053227
Maprs796053227
PheGenIrs796053227
hapmaprs796053227
1000 genomesrs796053227
hgdprs796053227
ensemblrs796053227
gopubmedrs796053227
geneviewrs796053227
scholarrs796053227
googlers796053227
pharmgkbrs796053227
gwascentralrs796053227
openSNPrs796053227
23andMers796053227
23andMe allrs796053227
SNP Nexus

SNPshotrs796053227
SNPdbers796053227
MSV3drs796053227
GWAS Ctlgrs796053227
Max Magnitude0
ClinVar
Risk rs796053227(T;T)
Alt rs796053227(T;T)
Reference rs796053227(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52200825C>T
CLNSRC
CLNACC RCV000189288.2,