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rs61752092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752092(C;T)
Make rs61752092(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position2406766
GenePEX10
is asnp
is mentioned by
dbSNPrs61752092
ebirs61752092
HLIrs61752092
Exacrs61752092
Varsomers61752092
Maprs61752092
PheGenIrs61752092
hapmaprs61752092
1000 genomesrs61752092
hgdprs61752092
ensemblrs61752092
gopubmedrs61752092
geneviewrs61752092
scholarrs61752092
googlers61752092
pharmgkbrs61752092
gwascentralrs61752092
openSNPrs61752092
23andMers61752092
23andMe allrs61752092
SNP Nexus

SNPshotrs61752092
SNPdbers61752092
MSV3drs61752092
GWAS Ctlgrs61752092
Max Magnitude0
ClinVar
Risk rs61752092(G,T;G,T)
Alt rs61752092(G,T;G,T)
Reference rs61752092(C;C)
Significance Pathogenic
Disease Peroxisome biogenesis disorder 6B
Variation info
Gene PEX10
CLNDBN Peroxisome biogenesis disorder 6B
Reversed 1
HGVS NC_000001.10:g.2338205G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149813.4,



[PMID 15542397] The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.