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: rs7604115
rs7604115
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3
2 233749470 intron variant C/T snv 0.37
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 1 2009 2015
dbSNP: rs11695484
rs11695484
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; DNAJB3
2 233745803 intron variant A/G snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 1 2012 2015
dbSNP: rs17864701
rs17864701
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; DNAJB3
2 233744071 intron variant C/T snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2015 2015
dbSNP: rs10929301
rs10929301
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; LOC100286922
2 233755003 splice region variant C/G;T snv 0.48
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 1 2009 2015
dbSNP: rs10929302
rs10929302
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; LOC100286922
2 233757136 intron variant G/A snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 1 2012 2015
dbSNP: rs11673726
rs11673726
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; LOC100286922
2 233755414 non coding transcript exon variant G/A;T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 1 2009 2015
dbSNP: rs35754645
rs35754645
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; LOC100286922
2 233755941 non coding transcript exon variant CTCT/-;CT delins 0.37
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs6714634
rs6714634
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; LOC100286922
2 233756119 non coding transcript exon variant T/C snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.800 1.000 1 2012 2015
dbSNP: rs6747843
rs6747843
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A3 ; LOC100286922
2 233755708 non coding transcript exon variant G/A snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2015 2015