Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10085588
rs10085588
SEM1 ; LOC105375411 ; LOC105375412
0.010 GeneticVariation BEFREE We provide functional regulatory evidence for the rs10085588, which may be a causal SNP within the 7q21.3 GWAS signal for osteoporosis. 30878523

2019