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

rs758020436

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758020436(C;T)
Make rs758020436(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position34992363
GenePDHX
is asnp
is mentioned by
dbSNPrs758020436
ebirs758020436
HLIrs758020436
Exacrs758020436
Varsomers758020436
Maprs758020436
PheGenIrs758020436
hapmaprs758020436
1000 genomesrs758020436
hgdprs758020436
ensemblrs758020436
gopubmedrs758020436
geneviewrs758020436
scholarrs758020436
googlers758020436
pharmgkbrs758020436
gwascentralrs758020436
openSNPrs758020436
23andMers758020436
23andMe allrs758020436
SNP Nexus

SNPshotrs758020436
SNPdbers758020436
MSV3drs758020436
GWAS Ctlgrs758020436
Max Magnitude0
ClinVar
Risk rs758020436(T;T)
Alt rs758020436(T;T)
Reference rs758020436(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PDHX
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.35013910C>T
CLNSRC
CLNACC RCV000196048.1,