RNF111, ring finger protein 111, 54778

N. diseases: 31; N. variants: 6
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: rs1044673
rs1044673 		15 59097267 3 prime UTR variant G/A snv 7.0E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1665050
rs1665050 		1.000 0.120 15 59001406 intron variant A/G;T snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs16940987
rs16940987 		15 59061664 intron variant C/A snv 0.17
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1401798992
rs1401798992 		1.000 0.120 15 58887316 missense variant G/C;T snv 7.0E-06
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 0
dbSNP: rs112129861
rs112129861 		1.000 0.040 15 59047450 intron variant G/A;C snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2899642
rs2899642 		0.925 0.120 15 59030849 missense variant C/G;T snv 0.36; 1.2E-05
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs2899642
rs2899642 		0.925 0.120 15 59030849 missense variant C/G;T snv 0.36; 1.2E-05
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2020 2020