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rs863224150

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224150(C;T)
Make rs863224150(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19353169
GenePDHA1
is asnp
is mentioned by
dbSNPrs863224150
ebirs863224150
HLIrs863224150
Exacrs863224150
Varsomers863224150
Maprs863224150
PheGenIrs863224150
hapmaprs863224150
1000 genomesrs863224150
hgdprs863224150
ensemblrs863224150
gopubmedrs863224150
geneviewrs863224150
scholarrs863224150
googlers863224150
pharmgkbrs863224150
gwascentralrs863224150
openSNPrs863224150
23andMers863224150
23andMe allrs863224150
SNP Nexus

SNPshotrs863224150
SNPdbers863224150
MSV3drs863224150
GWAS Ctlgrs863224150
Max Magnitude0
ClinVar
Risk rs863224150(T;T)
Alt rs863224150(T;T)
Reference rs863224150(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19371287C>T
CLNSRC
CLNACC RCV000199416.2,