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rs863224146

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224146(C;T)
Make rs863224146(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19358926
GenePDHA1
is asnp
is mentioned by
dbSNPrs863224146
ebirs863224146
HLIrs863224146
Exacrs863224146
Varsomers863224146
Maprs863224146
PheGenIrs863224146
hapmaprs863224146
1000 genomesrs863224146
hgdprs863224146
ensemblrs863224146
gopubmedrs863224146
geneviewrs863224146
scholarrs863224146
googlers863224146
pharmgkbrs863224146
gwascentralrs863224146
openSNPrs863224146
23andMers863224146
23andMe allrs863224146
SNP Nexus

SNPshotrs863224146
SNPdbers863224146
MSV3drs863224146
GWAS Ctlgrs863224146
Max Magnitude0
ClinVar
Risk rs863224146(T;T)
Alt rs863224146(T;T)
Reference rs863224146(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19377044C>T
CLNSRC
CLNACC RCV000196688.1,