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

rs61752133

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61752133(-;-)
Make rs61752133(-;T)
Make rs61752133(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position18079897
GenePEX26
is asnp
is mentioned by
dbSNPrs61752133
ebirs61752133
HLIrs61752133
Exacrs61752133
Varsomers61752133
Maprs61752133
PheGenIrs61752133
hapmaprs61752133
1000 genomesrs61752133
hgdprs61752133
ensemblrs61752133
gopubmedrs61752133
geneviewrs61752133
scholarrs61752133
googlers61752133
pharmgkbrs61752133
gwascentralrs61752133
openSNPrs61752133
23andMers61752133
23andMe allrs61752133
SNP Nexus

SNPshotrs61752133
SNPdbers61752133
MSV3drs61752133
GWAS Ctlgrs61752133
Max Magnitude0
ClinVar
Risk rs61752133(T;T)
Alt rs61752133(T;T)
Reference rs61752133(;)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 7B Peroxisome biogenesis disorder 7A
Variation info
Gene PEX26
CLNDBN Peroxisome biogenesis disorder 7B Peroxisome biogenesis disorder 7A
Reversed 0
HGVS NC_000022.10:g.18562663dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000002241.2, RCV000002243.2,