Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908094
rs121908094
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
0.010 GeneticVariation BEFREE We now report novel compound heterozygous mutations in exon 1 (c.121C>T; p.Q41X) and exon 6 (c.743C>T; p.P248L) in ZMPSTE24 in two Japanese sisters, 7- and 3-year old, with severe MAD and characteristic facies and atrophic skin. 18435794

2008

dbSNP: rs121908095
rs121908095
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
0.010 GeneticVariation BEFREE We now report novel compound heterozygous mutations in exon 1 (c.121C>T; p.Q41X) and exon 6 (c.743C>T; p.P248L) in ZMPSTE24 in two Japanese sisters, 7- and 3-year old, with severe MAD and characteristic facies and atrophic skin. 18435794

2008

dbSNP: rs281875371
rs281875371
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
0.010 GeneticVariation BEFREE We now report a 37-year-old Australian man with MAD who also had compound heterozygous mutations in the ZMPSTE24 gene, a null mutation, Phe361fsX379, and a missense mutation, Asn265Ser, which is partially active in the yeast complementation assay. 17152860

2006