Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057520608
rs1057520608
T 0.700 CausalMutation CLINVAR

dbSNP: rs11546829
rs11546829
T 0.700 CausalMutation CLINVAR

dbSNP: rs1227875610
rs1227875610
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554579004
rs1554579004
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554580140
rs1554580140
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554580142
rs1554580142
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554580149
rs1554580149
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554580153
rs1554580153
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554601476
rs1554601476
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1554601481
rs1554601481
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554601502
rs1554601502
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554601525
rs1554601525
GCA 0.700 CausalMutation CLINVAR

dbSNP: rs1554601526
rs1554601526
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554657940
rs1554657940
G 0.700 CausalMutation CLINVAR

dbSNP: rs1563569983
rs1563569983
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563571296
rs1563571296
GTTCCATATTAAACTGTTACGTGA 0.700 GeneticVariation CLINVAR

dbSNP: rs1563571318
rs1563571318
C 0.700 CausalMutation CLINVAR

dbSNP: rs1563575697
rs1563575697
TGA 0.700 CausalMutation CLINVAR

dbSNP: rs1563659352
rs1563659352
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563659571
rs1563659571
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563659649
rs1563659649
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1563659821
rs1563659821
C 0.700 CausalMutation CLINVAR

dbSNP: rs188859975
rs188859975
0.700 GeneticVariation UNIPROT

dbSNP: rs886039486
rs886039486
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554601568
rs1554601568
G 0.700 CausalMutation CLINVAR "Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of ""protective"" and ""risk"" factors." 22258776

2011