Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568689930
rs1568689930
AC 0.700 CausalMutation CLINVAR

dbSNP: rs1568689994
rs1568689994
A 0.700 CausalMutation CLINVAR

dbSNP: rs1568690161
rs1568690161
AT 0.700 CausalMutation CLINVAR

dbSNP: rs397518440
rs397518440
G 0.700 CausalMutation CLINVAR

dbSNP: rs397518441
rs397518441
GT 0.700 CausalMutation CLINVAR

dbSNP: rs397518443
rs397518443
G 0.700 CausalMutation CLINVAR

dbSNP: rs587776656
rs587776656
C 0.700 CausalMutation CLINVAR

dbSNP: rs587776657
rs587776657
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776658
rs587776658
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776659
rs587776659
C 0.700 CausalMutation CLINVAR

dbSNP: rs587776660
rs587776660
A 0.700 CausalMutation CLINVAR

dbSNP: rs727504172
rs727504172
C 0.700 CausalMutation CLINVAR

dbSNP: rs730881976
rs730881976
A 0.700 CausalMutation CLINVAR

dbSNP: rs730881976
rs730881976
G 0.700 GeneticVariation CLINVAR

dbSNP: rs778376925
rs778376925
G 0.700 CausalMutation CLINVAR

dbSNP: rs778376925
rs778376925
A 0.700 CausalMutation CLINVAR

dbSNP: rs786201213
rs786201213
A 0.700 CausalMutation CLINVAR

dbSNP: rs863224448
rs863224448
A 0.700 GeneticVariation CLINVAR

dbSNP: rs864622488
rs864622488
T 0.700 GeneticVariation CLINVAR

dbSNP: rs864622707
rs864622707
C 0.700 CausalMutation CLINVAR

dbSNP: rs878853247
rs878853247
T 0.700 GeneticVariation CLINVAR

dbSNP: rs886037859
rs886037859
G 0.700 CausalMutation CLINVAR

dbSNP: rs886037859
rs886037859
G 0.700 GeneticVariation CLINVAR

dbSNP: rs886037926
rs886037926
G 0.700 GeneticVariation CLINVAR

dbSNP: rs730881979
rs730881979
A 0.800 CausalMutation CLINVAR Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4. 9399902

1997