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: rs165975
rs165975
ABCC1
16 16040137 intron variant T/C snv 0.30
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs17264736
rs17264736
ABCC1
16 16022699 intron variant G/T snv 0.45
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs17264736
rs17264736
ABCC1
16 16022699 intron variant G/T snv 0.45
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs193538
rs193538
ABCC1
16 16034059 intron variant G/A;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs60782127
rs60782127
ABCC1
16 16048222 missense variant G/T snv 8.9E-03 7.6E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs74475935
rs74475935
ABCC1
1.000 0.080 16 15961249 intron variant C/G snv 4.5E-03
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.700 1.000 1 2016 2016
dbSNP: rs924135
rs924135
ABCC1
16 16029602 intron variant A/C;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016