AR, androgen receptor, 367

N. diseases: 854; N. variants: 163
Disease: Alopecia, Male Pattern ×
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: rs1204038
rs1204038 		0.882 0.160 X 67568383 intron variant G/A snv 0.36
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs12396249
rs12396249 		1.000 0.080 X 67557224 intron variant G/A snv 0.20
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1337080
rs1337080 		1.000 0.080 X 67659077 intron variant G/A snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2255702
rs2255702 		1.000 0.080 X 67578269 intron variant C/T snv 0.36
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4827545
rs4827545 		1.000 0.080 X 67608543 intron variant A/G;T snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5918757
rs5918757 		1.000 0.080 X 67586188 intron variant G/A snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5918760
rs5918760 		1.000 0.080 X 67618909 intron variant T/A;C snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5918762
rs5918762 		1.000 0.080 X 67694959 3 prime UTR variant T/C snv 0.64
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5918764
rs5918764 		1.000 0.080 X 67717865 intron variant A/G;T snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs5919393
rs5919393 		1.000 0.080 X 67605515 intron variant C/T snv 0.64
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6624304
rs6624304 		0.882 0.160 X 67655914 intron variant T/A;C snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6152
rs6152 		0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.020 1.000 2 2010 2015