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

rs398123300

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123300(C;T)
Make rs398123300(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position19353146
GenePDHA1
is asnp
is mentioned by
dbSNPrs398123300
ebirs398123300
HLIrs398123300
Exacrs398123300
Varsomers398123300
Maprs398123300
PheGenIrs398123300
hapmaprs398123300
1000 genomesrs398123300
hgdprs398123300
ensemblrs398123300
gopubmedrs398123300
geneviewrs398123300
scholarrs398123300
googlers398123300
pharmgkbrs398123300
gwascentralrs398123300
openSNPrs398123300
23andMers398123300
23andMe allrs398123300
SNP Nexus

SNPshotrs398123300
SNPdbers398123300
MSV3drs398123300
GWAS Ctlgrs398123300
Max Magnitude0
ClinVar
Risk rs398123300(T;T)
Alt rs398123300(T;T)
Reference rs398123300(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHA1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.19371264C>T
CLNSRC HGMD
CLNACC RCV000078557.4,