Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C0009081
Disease:
Congenital clubfoot 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C1859399
Disease:
Radial bowing 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C0345375
Disease:
Congenital hypoplasia of femur 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C1859461
Disease:
Femoral bowing 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C1851310
Disease:
Aplasia/hypoplasia of the femur 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C0432098
Disease:
Cleft Soft Palate 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C0685409
Disease:
Congenital Camptodactyly 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C1855340
Disease:
Bowing of the long bones 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs780770356
rs780770356
Entrez Id: 5352;109729161
Gene Symbol: PLOD2;LNCSRLR
PLOD2;LNCSRLR
CUI: C1865847
Disease:
Ulnar bowing 		A 0.700 GeneticVariation CLINVAR