Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312907
rs869312907
0.810 GeneticVariation BEFREE We suggest that the p.Gly207Arg variant causes a distinct type II collagenopathy with features of PPRD and SED, Stanescu type. 26183434

2015

dbSNP: rs869312907
rs869312907
T 0.810 CausalMutation CLINVAR

dbSNP: rs869312907
rs869312907
0.810 GeneticVariation UNIPROT