SLC22A3, solute carrier family 22 member 3, 6581

N. diseases: 154; N. variants: 30
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: rs7758229
rs7758229 		0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.810 0.500 2 2011 2013
dbSNP: rs9364554
rs9364554 		0.882 0.160 6 160412632 intron variant C/T snv 0.21
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.710 1.000 4 2008 2018
dbSNP: rs9364554
rs9364554 		0.882 0.160 6 160412632 intron variant C/T snv 0.21
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.710 1.000 2 2008 2012
dbSNP: rs7758229
rs7758229 		0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.710 1.000 1 2011 2011
dbSNP: rs2048327
rs2048327 		0.851 0.120 6 160442500 intron variant T/C snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 3 2009 2014
dbSNP: rs487152
rs487152 		6 160353454 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2017 2019
dbSNP: rs2048327
rs2048327 		0.851 0.120 6 160442500 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 2 2009 2014
dbSNP: rs668871
rs668871 		6 160348779 synonymous variant C/G;T snv 0.45 0.50
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2019 2019
dbSNP: rs1018234
rs1018234 		6 160375026 intron variant C/T snv 0.32
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs12194182
rs12194182 		1.000 0.040 6 160413483 intron variant T/C snv 0.21
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs12204009
rs12204009 		6 160378214 intron variant T/C snv 2.8E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs141463285
rs141463285 		6 160417614 intron variant T/A snv 4.2E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs143665477
rs143665477 		6 160446240 intron variant T/A;C snv
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs149302195
rs149302195 		6 160382662 intron variant C/T snv 2.5E-03
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs1567441
rs1567441 		6 160391230 intron variant T/C snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs189821701
rs189821701 		6 160441777 intron variant C/T snv 2.4E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2457574
rs2457574 		6 160447669 intron variant G/A snv 0.44 0.42
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3105749
rs3105749 		6 160399946 intron variant G/A snv 0.46
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3123636
rs3123636 		1.000 0.080 6 160421505 intron variant T/C;G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2016 2016
dbSNP: rs3127574
rs3127574 		6 160370338 non coding transcript exon variant C/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs376563
rs376563 		6 160430734 intron variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs376563
rs376563 		6 160430734 intron variant T/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs474513
rs474513 		6 160349280 intron variant A/G snv 0.51
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs520829
rs520829 		6 160346873 upstream gene variant T/G snv 0.51
CUI: C1096202
Disease: Lipoprotein (a) measurement
Lipoprotein (a) measurement 		0.700 1.000 1 2017 2017
dbSNP: rs543159
rs543159 		6 160354985 intron variant C/A snv 0.37
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 1 2019 2019