Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10459648
rs10459648
ARID3B
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs10905359
rs10905359
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs11263613
rs11263613
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs13089920
rs13089920
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs17090300
rs17090300
LINC00392 ; LINC00393 ; LOC107984024
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs17802111
rs17802111
LOC101926974
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs3754648
rs3754648
AGAP1
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs3923380
rs3923380
SHROOM3
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs4750407
rs4750407
FRMD4A
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs7420812
rs7420812
PARD3B
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016
dbSNP: rs754423
rs754423
NID2
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712

2016