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

rs863224148

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224148(C;T)
Make rs863224148(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position19350033
GenePDHA1
is asnp
is mentioned by
dbSNPrs863224148
ebirs863224148
HLIrs863224148
Exacrs863224148
Varsomers863224148
Maprs863224148
PheGenIrs863224148
hapmaprs863224148
1000 genomesrs863224148
hgdprs863224148
ensemblrs863224148
gopubmedrs863224148
geneviewrs863224148
scholarrs863224148
googlers863224148
pharmgkbrs863224148
gwascentralrs863224148
openSNPrs863224148
23andMers863224148
23andMe allrs863224148
SNP Nexus

SNPshotrs863224148
SNPdbers863224148
MSV3drs863224148
GWAS Ctlgrs863224148
Max Magnitude0
ClinVar
Risk rs863224148(T;T)
Alt rs863224148(T;T)
Reference rs863224148(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19368151C>T
CLNSRC
CLNACC RCV000196233.1,