Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606986
rs267606986
Entrez Id: 5744
Gene Symbol: PTHLH
PTHLH
CUI: C3150644
Disease:
BRACHYDACTYLY, TYPE E2
0.800 GeneticVariation UNIPROT Deletion and point mutations of PTHLH cause brachydactyly type E. 20170896 2010
dbSNP: rs267606986
rs267606986
Entrez Id: 5744
Gene Symbol: PTHLH
PTHLH
CUI: C3150644
Disease:
BRACHYDACTYLY, TYPE E2
G 0.800 CausalMutation CLINVAR