Source: ALL
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: rs119103270
rs119103270
NCF1
1 1.000 0.120 7 74777319 missense variant G/A snv 1.6E-05 0.700 0
dbSNP: rs119103271
rs119103271
NCF1
1 1.000 0.120 7 74779298 stop gained C/G;T snv 0.700 0
dbSNP: rs119103272
rs119103272
NCF1
1 1.000 0.120 7 74779360 stop gained T/A snv 0.700 0
dbSNP: rs119103273
rs119103273
NCF1
1 1.000 0.120 7 74783061 missense variant G/A snv 3.2E-05 0.700 0
dbSNP: rs1307080411
rs1307080411
NCF1
1 1.000 0.120 7 74787994 frameshift variant G/- del 0.700 0
dbSNP: rs145360423
rs145360423
NCF1
3 0.925 0.120 7 74783529 stop gained G/A snv 6.9E-04 5.3E-04 0.700 0
dbSNP: rs1563003964
rs1563003964
NCF1
1 1.000 0.120 7 74782989 frameshift variant G/- del 0.700 0
dbSNP: rs4029402
rs4029402
NCF1
2 1.000 0.120 7 74777267 frameshift variant GT/- delins 0.700 0