Disease: Serum Alanine Aminotransferase 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: rs738409
rs738409 		0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.800 1.000 3 2011 2018
dbSNP: rs12483959
rs12483959 		1.000 22 43930116 intron variant G/A;C;T snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 2 2011 2019
dbSNP: rs2281135
rs2281135 		0.851 0.160 22 43936690 intron variant G/A snv 0.19
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2008 2008
dbSNP: rs2294915
rs2294915 		1.000 0.040 22 43945024 intron variant C/G;T snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2896019
rs2896019 		0.790 0.160 22 43937814 intron variant T/G snv 0.20
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs3747207
rs3747207 		22 43928975 intron variant G/A snv 0.22
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4823173
rs4823173 		0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs738408
rs738408 		0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2017 2017