Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224158

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224158(A;A)
Make rs863224158(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position58430827
GenePDHB
is asnp
is mentioned by
dbSNPrs863224158
ebirs863224158
HLIrs863224158
Exacrs863224158
Varsomers863224158
Maprs863224158
PheGenIrs863224158
hapmaprs863224158
1000 genomesrs863224158
hgdprs863224158
ensemblrs863224158
gopubmedrs863224158
geneviewrs863224158
scholarrs863224158
googlers863224158
pharmgkbrs863224158
gwascentralrs863224158
openSNPrs863224158
23andMers863224158
23andMe allrs863224158
SNP Nexus

SNPshotrs863224158
SNPdbers863224158
MSV3drs863224158
GWAS Ctlgrs863224158
Max Magnitude0
ClinVar
Risk rs863224158(A;A)
Alt rs863224158(A;A)
Reference rs863224158(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDHB
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.58416554A>T
CLNSRC
CLNACC RCV000197569.1,