Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913483
rs121913483
G 0.820 CausalMutation CLINVAR

dbSNP: rs121913482
rs121913482
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913530
rs121913530
0.800 GeneticVariation UNIPROT

dbSNP: rs121913530
rs121913530
G 0.800 CausalMutation CLINVAR

dbSNP: rs78311289
rs78311289
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894228
rs104894228
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894229
rs104894229
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894230
rs104894230
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894230
rs104894230
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894360
rs104894360
A 0.700 CausalMutation CLINVAR

dbSNP: rs121434629
rs121434629
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913105
rs121913105
C 0.700 CausalMutation CLINVAR

dbSNP: rs137853294
rs137853294
RB1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555515731
rs1555515731
G 0.700 CausalMutation CLINVAR

dbSNP: rs28897728
rs28897728
0.700 GeneticVariation UNIPROT

dbSNP: rs28931614
rs28931614
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933068
rs28933068
G 0.700 CausalMutation CLINVAR

dbSNP: rs4647924
rs4647924
G 0.700 CausalMutation CLINVAR

dbSNP: rs587776783
rs587776783
A 0.700 CausalMutation CLINVAR

dbSNP: rs786201675
rs786201675
ATM
C 0.700 GeneticVariation CLINVAR

dbSNP: rs121913483
rs121913483
0.820 GeneticVariation UNIPROT Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas. 10471491

1999

dbSNP: rs121913482
rs121913482
0.800 GeneticVariation UNIPROT Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas. 10471491

1999

dbSNP: rs78311289
rs78311289
0.800 GeneticVariation UNIPROT Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas. 10471491

1999

dbSNP: rs121913479
rs121913479
0.700 GeneticVariation UNIPROT Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas. 10471491

1999

dbSNP: rs121913483
rs121913483
0.820 GeneticVariation UNIPROT Loss of heterozygosity at 4p16.3 and mutation of FGFR3 in transitional cell carcinoma. 11314002

2001