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rs863224157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224157(-;CTTGCCAGTGTGGA)
Make rs863224157(CTTGCCAGTGTGGA;CTTGCCAGTGTGGA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19359014
GenePDHA1
is asnp
is mentioned by
dbSNPrs863224157
ClinGenrs863224157
ebirs863224157
HLIrs863224157
Exacrs863224157
Varsomers863224157
Maprs863224157
PheGenIrs863224157
hapmaprs863224157
1000 genomesrs863224157
hgdprs863224157
ensemblrs863224157
gopubmedrs863224157
geneviewrs863224157
scholarrs863224157
googlers863224157
pharmgkbrs863224157
gwascentralrs863224157
openSNPrs863224157
23andMers863224157
23andMe allrs863224157
SNP Nexus

SNPshotrs863224157
SNPdbers863224157
MSV3drs863224157
GWAS Ctlgrs863224157
Max Magnitude0
ClinVar
Risk rs863224157(CTTGCCAGTGTGGA;CTTGCCAGTGTGGA)
Alt rs863224157(CTTGCCAGTGTGGA;CTTGCCAGTGTGGA)
Reference Rs863224157(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19377119_19377132dupCTTGCCAGTGTGGA
CLNSRC
CLNACC RCV000199933.1,