Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518879
rs1057518879
PLOD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518898
rs1057518898
DYNC2H1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518911
rs1057518911
COL2A1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121913482
rs121913482
FGFR3
T 0.700 CausalMutation CLINVAR

dbSNP: rs137853027
rs137853027
DYNC2H1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553827236
rs1553827236
CC2D2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554699491
rs1554699491
AGTPBP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565868973
rs1565868973
TRPV4
T 0.700 CausalMutation CLINVAR

dbSNP: rs201037487
rs201037487
FAM98C
T 0.700 GeneticVariation CLINVAR

dbSNP: rs386833760
rs386833760
CC2D2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs67394386
rs67394386
COL1A1
T 0.700 CausalMutation CLINVAR

dbSNP: rs758522600
rs758522600
BBS10
A 0.700 CausalMutation CLINVAR

dbSNP: rs780631499
rs780631499
AGTPBP1
C 0.700 CausalMutation CLINVAR

dbSNP: rs786205645
rs786205645
NEK1
C 0.700 CausalMutation CLINVAR

dbSNP: rs796052243
rs796052243
SPATA5
T 0.700 GeneticVariation CLINVAR

dbSNP: rs886039795
rs886039795
TMEM256 ; TMEM256-PLSCR3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886039806
rs886039806
KIAA0586
G 0.700 GeneticVariation CLINVAR

dbSNP: rs886039812
rs886039812
DYNC2H1
G 0.700 GeneticVariation CLINVAR