Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4647924
rs4647924
FGFR3
G 0.710 CausalMutation CLINVAR

dbSNP: rs1014959895
rs1014959895
PRMT7
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894396
rs104894396
GJB2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518907
rs1057518907
GNAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518972
rs1057518972
TRPS1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519324
rs1057519324
NPR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057520063
rs1057520063
GLI3
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1251713297
rs1251713297
PRMT7
A 0.700 CausalMutation CLINVAR

dbSNP: rs137853027
rs137853027
DYNC2H1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs137854539
rs137854539
GNAS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1400419650
rs1400419650
TRIP11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553154130
rs1553154130
RERE
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554888939
rs1554888939
EHMT1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555154946
rs1555154946
ARID2 ; LOC105369745
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555386022
rs1555386022
TRIP11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555528356
rs1555528356
ANKRD11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556165162
rs1556165162
HDAC8
T 0.700 CausalMutation CLINVAR

dbSNP: rs1565311145
rs1565311145
DYNC2H1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565317399
rs1565317399
DYNC2H1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567690011
rs1567690011
PRMT7
C 0.700 CausalMutation CLINVAR

dbSNP: rs1567721991
rs1567721991
PRMT7
TGCTCTCCG 0.700 CausalMutation CLINVAR

dbSNP: rs368869806
rs368869806
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs371011047
rs371011047
DYNC2H1
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906836
rs387906836
TULP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507520
rs397507520
PTPN11
C 0.700 CausalMutation CLINVAR