Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs312262900
rs312262900
Entrez Id: 1311
Gene Symbol: COMP
COMP
CUI: C0410538
Disease:
Pseudoachondroplasia
A 0.700 CausalMutation CLINVAR
dbSNP: rs312262900
rs312262900
Entrez Id: 1311
Gene Symbol: COMP
COMP
CUI: C0410538
Disease:
Pseudoachondroplasia
C 0.700 CausalMutation CLINVAR
dbSNP: rs312262900
rs312262900
Entrez Id: 1311
Gene Symbol: COMP
COMP
CUI: C0410538
Disease:
Pseudoachondroplasia
T 0.700 CausalMutation CLINVAR