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rs61752129

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61752129(-;-)
Make rs61752129(-;C)
Make rs61752129(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position18078410
GenePEX26
is asnp
is mentioned by
dbSNPrs61752129
ebirs61752129
HLIrs61752129
Exacrs61752129
Varsomers61752129
Maprs61752129
PheGenIrs61752129
hapmaprs61752129
1000 genomesrs61752129
hgdprs61752129
ensemblrs61752129
gopubmedrs61752129
geneviewrs61752129
scholarrs61752129
googlers61752129
pharmgkbrs61752129
gwascentralrs61752129
openSNPrs61752129
23andMers61752129
23andMe allrs61752129
SNP Nexus

SNPshotrs61752129
SNPdbers61752129
MSV3drs61752129
GWAS Ctlgrs61752129
Max Magnitude0
ClinVar
Risk rs61752129(C;C)
Alt rs61752129(C;C)
Reference rs61752129(;)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 7A
Variation info
Gene PEX26
CLNDBN Peroxisome biogenesis disorder 7A
Reversed 0
HGVS NC_000022.10:g.18561176dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000002237.2,