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rs61752103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752103(C;T)
Make rs61752103(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position35577180
GenePEX12
is asnp
is mentioned by
dbSNPrs61752103
ebirs61752103
HLIrs61752103
Exacrs61752103
Varsomers61752103
Maprs61752103
PheGenIrs61752103
hapmaprs61752103
1000 genomesrs61752103
hgdprs61752103
ensemblrs61752103
gopubmedrs61752103
geneviewrs61752103
scholarrs61752103
googlers61752103
pharmgkbrs61752103
gwascentralrs61752103
openSNPrs61752103
23andMers61752103
23andMe allrs61752103
SNP Nexus

SNPshotrs61752103
SNPdbers61752103
MSV3drs61752103
GWAS Ctlgrs61752103
Max Magnitude0
OMIM601758
Desc
Variant0005
Relatedalso


ClinVar
Risk rs61752103(G,T;G,T)
Alt rs61752103(G,T;G,T)
Reference rs61752103(C;C)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 3A Peroxisomal biogenesis disorder 3b
Variation info
Gene PEX12
CLNDBN Peroxisome biogenesis disorder 3A Peroxisomal biogenesis disorder 3b
Reversed 1
HGVS NC_000017.10:g.33904199G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008216.2, RCV000032926.2,