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rs61752128

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61752128(C;C)
Make rs61752128(C;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position76983440
GenePEX2
is asnp
is mentioned by
dbSNPrs61752128
ebirs61752128
HLIrs61752128
Exacrs61752128
Varsomers61752128
Maprs61752128
PheGenIrs61752128
hapmaprs61752128
1000 genomesrs61752128
hgdprs61752128
ensemblrs61752128
gopubmedrs61752128
geneviewrs61752128
scholarrs61752128
googlers61752128
pharmgkbrs61752128
gwascentralrs61752128
openSNPrs61752128
23andMers61752128
23andMe allrs61752128
SNP Nexus

SNPshotrs61752128
SNPdbers61752128
MSV3drs61752128
GWAS Ctlgrs61752128
Max Magnitude0


ClinVar
Risk rs61752128(C;C)
Alt rs61752128(C;C)
Reference rs61752128(T;T)
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.77895676A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128530.2,