SLC23A2, solute carrier family 23 member 2, 9962

N. diseases: 46; N. variants: 10
Disease: Acute Coronary Syndrome ×
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: rs1776964
rs1776964 		1.000 0.040 20 4899662 synonymous variant G/A snv 0.47 0.45
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6139591
rs6139591 		1.000 0.040 20 4970713 intron variant G/A snv 0.40
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2013 2013