Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs765379963
rs765379963
TMCO1
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C1860493
Disease: Abnormality of the sternum
Abnormality of the sternum 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0038379
Disease: Strabismus
Strabismus 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0542519
Disease: Congenital absence of kidney
Congenital absence of kidney 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C1301509
Disease: Severe visual impairment
Severe visual impairment 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0265677
Disease: Congenital hemivertebra
Congenital hemivertebra 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C1398522
Disease: Cleft palate and bilateral cleft lip
Cleft palate and bilateral cleft lip 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C3553084
Disease: Bilateral cleft palate
Bilateral cleft palate 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
CUI: C0392005
Disease: Bilateral cleft lip
Bilateral cleft lip 		A 0.700 CausalMutation CLINVAR