PRL, prolactin, 5617

N. diseases: 506; N. variants: 3
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: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.020 1.000 2 2009 2019
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0026618
Disease: Dental Fluorosis, Acquired
Dental Fluorosis, Acquired
Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0020514
Disease: Hyperprolactinemia
Hyperprolactinemia
Nervous System Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid
Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris
Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1341239
rs1341239
0.776 0.360 6 22303975 intron variant A/C snv 0.65
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs3756824
rs3756824
0.925 0.080 6 22298508 intron variant C/G;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3756824
rs3756824
0.925 0.080 6 22298508 intron variant C/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3756824
rs3756824
0.925 0.080 6 22298508 intron variant C/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs768767532
rs768767532
1.000 0.040 6 22296961 missense variant A/G snv 4.0E-06
CUI: C0004509
Disease: Azoospermia
Azoospermia
Male Urogenital Diseases 0.010 < 0.001 1 2003 2003