Source: BEFREE ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799864
rs1799864
CCR2
66 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2015 2015
dbSNP: rs1799969
rs1799969
ICAM1
38 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.010 1.000 1 2017 2017
dbSNP: rs374161061
rs374161061
HSD17B4
2 1.000 0.280 5 119499543 missense variant A/G snv 1.2E-04 2.1E-05 0.010 1.000 1 2017 2017
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
97 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2017 2017
dbSNP: rs770917763
rs770917763
TWNK ; MRPL43
1 10 100989178 missense variant G/A;T snv 1.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs863223921
rs863223921
TWNK ; MRPL43
2 0.925 0.280 10 100989406 missense variant A/G snv 4.0E-06 1.4E-05 0.010 1.000 1 2017 2017