ITGB8, integrin subunit beta 8, 3696

N. diseases: 14; N. variants: 14
Source: GWASCAT ×
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: rs10231365
rs10231365 		7 20391962 intron variant C/T snv 0.57
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs10486391
rs10486391 		1.000 0.080 7 20336395 intron variant A/G snv 0.37
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11452686
rs11452686 		1.000 0.080 7 20374488 intron variant AAAAA/-;A;AAA;AAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAAAAAAAA delins
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs149317277
rs149317277 		0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs149317277
rs149317277 		0.925 0.080 7 20384300 intron variant -/GAAACAAGATTCT;GAACCAAGATTCT delins 0.36
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17365498
rs17365498 		7 20399351 intron variant T/C snv 0.68
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs17455862
rs17455862 		0.925 0.040 7 20362635 intron variant T/C snv 0.25
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs17455862
rs17455862 		0.925 0.040 7 20362635 intron variant T/C snv 0.25
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2040732
rs2040732 		1.000 0.040 7 20378511 intron variant C/T snv 0.39
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2214442
rs2214442 		7 20353164 non coding transcript exon variant A/G snv 0.53
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2214442
rs2214442 		7 20353164 non coding transcript exon variant A/G snv 0.53
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs3757727
rs3757727 		1.000 0.080 7 20372274 intron variant T/C snv 0.38
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3807931
rs3807931 		7 20342051 intron variant G/A snv 0.52
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3807945
rs3807945 		7 20376203 intron variant G/A snv 0.55
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3823974
rs3823974 		7 20403173 intron variant T/C snv 0.35
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs4473914
rs4473914 		1.000 0.080 7 20386640 intron variant T/C snv 0.37
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6955431
rs6955431 		7 20404437 intron variant T/C snv 0.23
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019