BMP6, bone morphogenetic protein 6, 654

N. diseases: 137; N. variants: 10
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: rs3812163
rs3812163 		6 7725527 upstream gene variant A/T snv 0.38
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs10498672
rs10498672 		6 7797607 intron variant C/G snv 0.13
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs10498672
rs10498672 		6 7797607 intron variant C/G snv 0.13
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs12215656
rs12215656 		6 7828976 intron variant G/A snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs140013431
rs140013431 		1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs270417
rs270417 		6 7729381 intron variant C/T snv 0.79
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs3812163
rs3812163 		6 7725527 upstream gene variant A/T snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs3812163
rs3812163 		6 7725527 upstream gene variant A/T snv 0.38
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs6923462
rs6923462 		6 7800879 intron variant T/C snv 0.20
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2014 2014
dbSNP: rs9505270
rs9505270 		1.000 0.040 6 7743430 intron variant G/A snv 0.29
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative 		Eye Diseases 0.700 1.000 1 2012 2012
dbSNP: rs909733732
rs909733732 		1.000 0.080 6 7880228 missense variant C/T snv 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1225934
rs1225934 		1.000 0.040 6 7877186 intron variant A/C snv 0.54
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs7745236
rs7745236 		1.000 0.040 6 7727292 missense variant C/G snv 4.9E-06; 4.1E-03 1.0E-02
CUI: C0282193
Disease: Iron Overload
Iron Overload 		Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016