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: rs137853045
rs137853045
1 1.000 0.240 12 49185804 missense variant T/G snv 0.800 1.000 2 2007 2015
dbSNP: rs137853046
rs137853046
1 1.000 0.240 12 49185579 missense variant G/T snv 0.800 1.000 2 2007 2015
dbSNP: rs137853047
rs137853047
1 1.000 0.240 12 49185110 missense variant G/A snv 0.800 1.000 2 2007 2015
dbSNP: rs137853050
rs137853050
1 1.000 0.240 12 49185101 missense variant C/T snv 0.700 1.000 2 2008 2010
dbSNP: rs1565627727
rs1565627727
1 1.000 0.240 12 49186670 missense variant G/A snv 0.700 1.000 1 2014 2014
dbSNP: rs753719501
rs753719501
1 1.000 0.240 12 49185142 stop gained G/A;T snv 1.2E-05 0.700 1.000 1 2016 2016
dbSNP: rs137853048
rs137853048
1 1.000 0.240 12 49185176 missense variant A/G snv 0.700 0
dbSNP: rs1555162242
rs1555162242
1 1.000 0.240 12 49185062 missense variant A/G snv 0.700 0
dbSNP: rs1555162294
rs1555162294
1 1.000 0.240 12 49185222 missense variant T/C snv 0.700 0
dbSNP: rs1555162456
rs1555162456
1 1.000 0.240 12 49186317 missense variant C/T snv 0.700 0
dbSNP: rs1565627072
rs1565627072
1 1.000 0.240 12 49185404 missense variant C/T snv 0.700 0
dbSNP: rs1565627513
rs1565627513
1 1.000 0.240 12 49186364 missense variant G/C snv 0.700 0
dbSNP: rs587784481
rs587784481
1 1.000 0.240 12 49185237 missense variant T/C snv 0.700 0
dbSNP: rs587784484
rs587784484
1 1.000 0.240 12 49185092 missense variant A/T snv 0.700 0
dbSNP: rs587784485
rs587784485
1 1.000 0.240 12 49186685 missense variant G/A snv 0.700 0
dbSNP: rs587784486
rs587784486
1 1.000 0.240 12 49186675 missense variant A/T snv 0.700 0
dbSNP: rs587784488
rs587784488
1 1.000 0.240 12 49185885 missense variant A/C;G snv 0.700 0
dbSNP: rs587784489
rs587784489
1 1.000 0.240 12 49185845 missense variant G/A snv 0.700 0
dbSNP: rs587784492
rs587784492
1 1.000 0.240 12 49185668 missense variant T/C snv 0.700 0
dbSNP: rs587784494
rs587784494
1 1.000 0.240 12 49185558 missense variant C/A;T snv 0.700 0
dbSNP: rs587784495
rs587784495
1 1.000 0.240 12 49185380 missense variant T/C snv 0.700 0
dbSNP: rs587784497
rs587784497
1 1.000 0.240 12 49185371 missense variant A/G snv 0.700 0
dbSNP: rs797046071
rs797046071
1 1.000 0.240 12 49185261 missense variant C/T snv 0.700 0
dbSNP: rs797046072
rs797046072
1 1.000 0.240 12 49186416 missense variant T/C snv 0.700 0
dbSNP: rs797046073
rs797046073
1 1.000 0.240 12 49185396 missense variant C/G snv 0.700 0