RGS17, regulator of G protein signaling 17, 26575

N. diseases: 35; 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: rs1933488
rs1933488 		0.925 0.080 6 153119944 intron variant A/G snv 0.45
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 2 2013 2018
dbSNP: rs2185027
rs2185027 		6 153060487 intron variant A/C snv 0.38
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2018
dbSNP: rs12055786
rs12055786 		6 153109990 intron variant C/T snv 0.46
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12055786
rs12055786 		6 153109990 intron variant C/T snv 0.46
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs12055786
rs12055786 		6 153109990 intron variant C/T snv 0.46
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result 		0.700 1.000 1 2012 2012
dbSNP: rs1281962
rs1281962 		6 153110241 intron variant G/C snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs1933264
rs1933264 		6 153070483 intron variant T/C snv 0.27
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1933488
rs1933488 		0.925 0.080 6 153119944 intron variant A/G snv 0.45
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2013 2013
dbSNP: rs503366
rs503366 		6 153012415 intron variant T/C snv 0.48
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs676199
rs676199 		6 153086711 intron variant T/A snv 0.40
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6913406
rs6913406 		6 153065807 intron variant G/A;C snv 0.38
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7749708
rs7749708 		6 153054772 intron variant C/T snv 0.39
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7749708
rs7749708 		6 153054772 intron variant C/T snv 0.39
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9397585
rs9397585 		6 153075740 intron variant T/C snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs9479509
rs9479509 		6 153106130 intron variant G/A snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9479509
rs9479509 		6 153106130 intron variant G/A snv 0.32
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs4083914
rs4083914 		0.882 0.080 6 153106571 intron variant C/G snv 0.46
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4083914
rs4083914 		0.882 0.080 6 153106571 intron variant C/G snv 0.46
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4083914
rs4083914 		0.882 0.080 6 153106571 intron variant C/G snv 0.46
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2012 2012