Gene: HPGD ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434480
rs121434480
HPGD
G 0.800 CausalMutation CLINVAR

dbSNP: rs587777719
rs587777719
HPGD
C 0.700 CausalMutation CLINVAR Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up. 24816859

2014
dbSNP: rs375335006
rs375335006
HPGD
C 0.700 GeneticVariation CLINVAR

dbSNP: rs548208942
rs548208942
HPGD ; LOC105377548
C 0.700 CausalMutation CLINVAR

dbSNP: rs577045722
rs577045722
HPGD ; LOC105377548
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776676
rs587776676
HPGD
TG 0.700 CausalMutation CLINVAR