PHF19, PHD finger protein 19, 26147

N. diseases: 28; N. variants: 12
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: rs10985070
rs10985070 		1.000 0.120 9 120873843 intron variant C/A snv 0.47
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 2 2014 2019
dbSNP: rs881375
rs881375 		0.925 0.160 9 120890620 intron variant T/C snv 0.68
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 2 2007 2009
dbSNP: rs1953126
rs1953126 		1.000 0.120 9 120878222 intron variant T/C snv 0.68
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs1953126
rs1953126 		1.000 0.120 9 120878222 intron variant T/C snv 0.68
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.800 1.000 1 2011 2011
dbSNP: rs2072438
rs2072438 		1.000 0.120 9 120889023 intron variant T/C snv 0.45
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 1 2014 2014
dbSNP: rs1953126
rs1953126 		1.000 0.120 9 120878222 intron variant T/C snv 0.68
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.710 1.000 3 2007 2009
dbSNP: rs10985073
rs10985073 		1.000 0.120 9 120881577 intron variant T/C snv 0.44
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs10760123
rs10760123 		9 120888256 intron variant T/A;G snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10760126
rs10760126 		1.000 0.120 9 120900340 downstream gene variant T/C snv 0.44
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs3933326
rs3933326 		9 120871670 intron variant A/G snv 0.65
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs59482735
rs59482735 		9 120881148 intron variant -/A;AA;AATA;AATTG ins 1.8E-03
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6478484
rs6478484 		1.000 0.040 9 120890102 intron variant T/A;C snv
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7847628
rs7847628 		9 120868947 intron variant A/C;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7847628
rs7847628 		9 120868947 intron variant A/C;G snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2016 2016
dbSNP: rs881375
rs881375 		0.925 0.160 9 120890620 intron variant T/C snv 0.68
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4836834
rs4836834 		1.000 0.120 9 120903623 3 prime UTR variant T/A snv 0.44
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016