ABCA1, ATP binding cassette subfamily A member 1, 19

N. diseases: 291; N. variants: 116
Disease: Triglycerides measurement ×
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: rs12686004
rs12686004 		1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1799777
rs1799777 		9 104903754 5 prime UTR variant -/C delins 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1800978
rs1800978 		1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1883025
rs1883025 		0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2575876
rs2575876 		9 104903458 intron variant G/A snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2740488
rs2740488 		0.827 0.120 9 104899461 intron variant A/C snv 0.29
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35207495
rs35207495 		9 104824519 missense variant C/T snv 1.2E-03 4.9E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3847303
rs3847303 		9 104886371 intron variant C/T snv 0.15
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009