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rs796053220

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053220(C;T)
Make rs796053220(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51790450
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053220
ebirs796053220
HLIrs796053220
Exacrs796053220
Varsomers796053220
Maprs796053220
PheGenIrs796053220
hapmaprs796053220
1000 genomesrs796053220
hgdprs796053220
ensemblrs796053220
gopubmedrs796053220
geneviewrs796053220
scholarrs796053220
googlers796053220
pharmgkbrs796053220
gwascentralrs796053220
openSNPrs796053220
23andMers796053220
23andMe allrs796053220
SNP Nexus

SNPshotrs796053220
SNPdbers796053220
MSV3drs796053220
GWAS Ctlgrs796053220
Max Magnitude0
ClinVar
Risk rs796053220(T;T)
Alt rs796053220(T;T)
Reference rs796053220(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52184234C>T
CLNSRC
CLNACC RCV000189281.2,