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rs863224145

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224145(A;A)
Make rs863224145(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19355452
GenePDHA1
is asnp
is mentioned by
dbSNPrs863224145
ebirs863224145
HLIrs863224145
Exacrs863224145
Varsomers863224145
Maprs863224145
PheGenIrs863224145
hapmaprs863224145
1000 genomesrs863224145
hgdprs863224145
ensemblrs863224145
gopubmedrs863224145
geneviewrs863224145
scholarrs863224145
googlers863224145
pharmgkbrs863224145
gwascentralrs863224145
openSNPrs863224145
23andMers863224145
23andMe allrs863224145
SNP Nexus

SNPshotrs863224145
SNPdbers863224145
MSV3drs863224145
GWAS Ctlgrs863224145
Max Magnitude0
ClinVar
Risk rs863224145(A;A)
Alt rs863224145(A;A)
Reference rs863224145(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19373570C>A
CLNSRC
CLNACC RCV000197492.1,