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: rs1014283
rs1014283
ABCB4
7 87447271 intron variant C/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1014283
rs1014283
ABCB4
7 87447271 intron variant C/A;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1558375
rs1558375
ABCB4
1.000 0.080 7 87449753 intron variant T/C snv 0.27
CUI: C0016978
Disease: gallbladder neoplasm
gallbladder neoplasm 		0.700 1.000 1 2017 2017
dbSNP: rs2109505
rs2109505
ABCB4
0.851 0.200 7 87450090 splice region variant T/A snv 0.21 0.22
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2109505
rs2109505
ABCB4
0.851 0.200 7 87450090 splice region variant T/A snv 0.21 0.22
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4148808
rs4148808
ABCB4
7 87476479 intron variant T/C snv 0.19
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018