rs78311289, FGFR3

N. diseases: 25
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acanthosis Nigricans
CUI: C0000889
Disease: Acanthosis Nigricans
0.720 GeneticVariation BEFREE Acanthosis nigricans and hypochondroplasia in a child with a K650Q mutation in FGFR3. 21510009 2011
Acanthosis Nigricans
CUI: C0000889
Disease: Acanthosis Nigricans
0.720 GeneticVariation BEFREE Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene. 18000903 2007
Acanthosis Nigricans
CUI: C0000889
Disease: Acanthosis Nigricans
0.720 GeneticVariation CLINVAR Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene. 18000903 2007