Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1021662947
rs1021662947
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057517539
rs1057517539
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057517600
rs1057517600
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057520645
rs1057520645
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499812
rs1060499812
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499813
rs1060499813
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060499814
rs1060499814
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499815
rs1060499815
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1060499818
rs1060499818
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060499819
rs1060499819
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499821
rs1060499821
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499823
rs1060499823
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060499824
rs1060499824
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499827
rs1060499827
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499828
rs1060499828
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499830
rs1060499830
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499831
rs1060499831
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502726
rs1060502726
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502734
rs1060502734
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060502759
rs1060502759
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502760
rs1060502760
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502800
rs1060502800
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502804
rs1060502804
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1064795824
rs1064795824
A 0.700 CausalMutation CLINVAR

dbSNP: rs118203997
rs118203997
T 0.700 CausalMutation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015