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rs796053219

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053219(A;A)
Make rs796053219(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51790420
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053219
ebirs796053219
HLIrs796053219
Exacrs796053219
Varsomers796053219
Maprs796053219
PheGenIrs796053219
hapmaprs796053219
1000 genomesrs796053219
hgdprs796053219
ensemblrs796053219
gopubmedrs796053219
geneviewrs796053219
scholarrs796053219
googlers796053219
pharmgkbrs796053219
gwascentralrs796053219
openSNPrs796053219
23andMers796053219
23andMe allrs796053219
SNP Nexus

SNPshotrs796053219
SNPdbers796053219
MSV3drs796053219
GWAS Ctlgrs796053219
Max Magnitude0
ClinVar
Risk rs796053219(A;A)
Alt rs796053219(A;A)
Reference rs796053219(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52184204T>A
CLNSRC
CLNACC RCV000189280.1,