Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12633863
rs12633863
TM4SF4
3 149493725 intron variant G/A snv 0.43
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018
dbSNP: rs28502438
rs28502438
TM4SF4
3 149502322 intron variant T/C snv 0.30
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2018 2018
dbSNP: rs60388273
rs60388273
TM4SF4
3 149496756 intron variant G/A snv 9.2E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs62269283
rs62269283
TM4SF4
3 149494481 intron variant G/A snv 1.9E-02
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs62269283
rs62269283
TM4SF4
3 149494481 intron variant G/A snv 1.9E-02
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6774054
rs6774054
TM4SF4
3 149493912 intron variant G/A snv 7.5E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs73152651
rs73152651
TM4SF4
3 149496397 intron variant G/T snv 7.8E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs9857970
rs9857970
TM4SF4
3 149492656 intron variant T/C snv 0.48
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.700 1.000 1 2018 2018