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: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.020 1.000 2 2015 2015
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.020 1.000 2 2015 2015
dbSNP: rs2030324
rs2030324
6 0.827 0.120 11 27705368 intron variant A/G snv 0.49 0.010 1.000 1 2005 2005
dbSNP: rs6484320
rs6484320
2 1.000 0.080 11 27681641 intron variant T/A;G snv 0.010 1.000 1 2005 2005
dbSNP: rs7934165
rs7934165
2 0.925 0.160 11 27710436 intron variant G/A snv 0.49 0.010 1.000 1 2005 2005