Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1206843725
rs1206843725
A 0.800 CausalMutation CLINVAR

dbSNP: rs137852825
rs137852825
T 0.800 CausalMutation CLINVAR

dbSNP: rs137852826
rs137852826
T 0.800 CausalMutation CLINVAR

dbSNP: rs137852827
rs137852827
G 0.800 CausalMutation CLINVAR

dbSNP: rs137852828
rs137852828
A 0.800 CausalMutation CLINVAR

dbSNP: rs267606802
rs267606802
T 0.800 CausalMutation CLINVAR

dbSNP: rs28931602
rs28931602
C 0.800 CausalMutation CLINVAR

dbSNP: rs794727560
rs794727560
T 0.800 CausalMutation CLINVAR

dbSNP: rs1057519320
rs1057519320
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519321
rs1057519321
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060503498
rs1060503498
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060503510
rs1060503510
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060503511
rs1060503511
T 0.700 GeneticVariation CLINVAR

dbSNP: rs138303817
rs138303817
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554122802
rs1554122802
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554122897
rs1554122897
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554123139
rs1554123139
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1561461125
rs1561461125
C 0.700 CausalMutation CLINVAR

dbSNP: rs1561758622
rs1561758622
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776519
rs587776519
C 0.700 CausalMutation CLINVAR

dbSNP: rs863223567
rs863223567
0.700 GeneticVariation UNIPROT

dbSNP: rs869025428
rs869025428
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1206843725
rs1206843725
0.800 GeneticVariation UNIPROT A novel FBN2 mutation in a Chinese family with congenital contractural arachnodactyly. 25834781

2015

dbSNP: rs137852825
rs137852825
0.800 GeneticVariation UNIPROT A novel FBN2 mutation in a Chinese family with congenital contractural arachnodactyly. 25834781

2015

dbSNP: rs137852826
rs137852826
0.800 GeneticVariation UNIPROT A novel FBN2 mutation in a Chinese family with congenital contractural arachnodactyly. 25834781

2015