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rs61752122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAGAT;GAGAT) 0 common in clinvar
Make rs61752122(-;-)
Make rs61752122(-;GAGAT)
ReferenceGRCh38 38.1/142
Chromosome8
Position76983896
GenePEX2
is asnp
is mentioned by
dbSNPrs61752122
ebirs61752122
HLIrs61752122
Exacrs61752122
Varsomers61752122
Maprs61752122
PheGenIrs61752122
hapmaprs61752122
1000 genomesrs61752122
hgdprs61752122
ensemblrs61752122
gopubmedrs61752122
geneviewrs61752122
scholarrs61752122
googlers61752122
pharmgkbrs61752122
gwascentralrs61752122
openSNPrs61752122
23andMers61752122
23andMe allrs61752122
SNP Nexus

SNPshotrs61752122
SNPdbers61752122
MSV3drs61752122
GWAS Ctlgrs61752122
Max Magnitude0
ClinVar
Risk rs61752122(;)
Alt rs61752122(;)
Reference rs61752122(GAGAT;GAGAT)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 5a (zellweger)
Variation info
Gene PEX2
CLNDBN Peroxisome biogenesis disorder 5a (zellweger)
Reversed 1
HGVS NC_000008.10:g.77896132_77896136delATCTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000128529.3,