TMEM182, transmembrane protein 182, 130827

N. diseases: 11; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10202535
rs10202535 		2 102957679 intron variant T/C snv 0.61
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12105421
rs12105421 		1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs12105421
rs12105421 		1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02
CUI: C0029516
Disease: Other and unspecified reactive psychosis
Other and unspecified reactive psychosis 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs2732860
rs2732860 		2 102781875 intron variant G/A snv 0.55
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2018 2018
dbSNP: rs4380261
rs4380261 		2 102962092 intron variant G/T snv 0.61
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62153409
rs62153409 		2 102778250 intron variant C/T snv 2.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs6752950
rs6752950 		0.925 0.040 2 102816833 3 prime UTR variant C/A;G snv 4.5E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs6752950
rs6752950 		0.925 0.040 2 102816833 3 prime UTR variant C/A;G snv 4.5E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs869833
rs869833 		1.000 0.040 2 102766672 intron variant T/C snv 0.49
CUI: C0017601
Disease: Glaucoma
Glaucoma 		Eye Diseases 0.010 < 0.001 1 2013 2013