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

rs61752127

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61752127(A;A)
Make rs61752127(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position76983510
GenePEX2
is asnp
is mentioned by
dbSNPrs61752127
ebirs61752127
HLIrs61752127
Exacrs61752127
Varsomers61752127
Maprs61752127
PheGenIrs61752127
hapmaprs61752127
1000 genomesrs61752127
hgdprs61752127
ensemblrs61752127
gopubmedrs61752127
geneviewrs61752127
scholarrs61752127
googlers61752127
pharmgkbrs61752127
gwascentralrs61752127
openSNPrs61752127
23andMers61752127
23andMe allrs61752127
SNP Nexus

SNPshotrs61752127
SNPdbers61752127
MSV3drs61752127
GWAS Ctlgrs61752127
Max Magnitude0


ClinVar
Risk rs61752127(A;A)
Alt rs61752127(A;A)
Reference rs61752127(G;G)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 5B
Variation info
Gene PEX2
CLNDBN Peroxisome biogenesis disorder 5B
Reversed 1
HGVS NC_000008.10:g.77895746C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128531.2,