Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057516127
rs1057516127
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519661
rs1057519661
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519677
rs1057519677
G 0.700 CausalMutation CLINVAR

dbSNP: rs112029328
rs112029328
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131692189
rs1131692189
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692190
rs1131692190
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692191
rs1131692191
CCATTCTG 0.700 CausalMutation CLINVAR

dbSNP: rs1131692192
rs1131692192
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131692193
rs1131692193
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692194
rs1131692194
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692195
rs1131692195
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1131692196
rs1131692196
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692197
rs1131692197
G 0.700 CausalMutation CLINVAR

dbSNP: rs1131692198
rs1131692198
AACTGCGGTAAACTGCGGTAAACT 0.700 CausalMutation CLINVAR

dbSNP: rs1131692200
rs1131692200
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131692201
rs1131692201
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131692202
rs1131692202
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131692213
rs1131692213
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692214
rs1131692214
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692215
rs1131692215
CTTG 0.700 CausalMutation CLINVAR

dbSNP: rs1131692216
rs1131692216
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692217
rs1131692217
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1131692219
rs1131692219
G 0.700 CausalMutation CLINVAR

dbSNP: rs1131692220
rs1131692220
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131692221
rs1131692221
T 0.700 CausalMutation CLINVAR