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: rs363853
rs363853
1 1.000 0.160 15 48596292 missense variant A/G snv 0.800 1.000 34 1993 2017
dbSNP: rs137854462
rs137854462
1 1.000 0.160 15 48510115 missense variant T/A snv 0.810 1.000 31 1993 2017
dbSNP: rs137854458
rs137854458
1 1.000 0.160 15 48483910 missense variant C/G snv 0.800 1.000 30 1993 2017
dbSNP: rs137854459
rs137854459
1 1.000 0.160 15 48463977 missense variant A/G snv 0.800 1.000 30 1993 2017
dbSNP: rs137854463
rs137854463
1 1.000 0.160 15 48497391 missense variant T/G snv 0.800 1.000 30 1993 2017
dbSNP: rs137854469
rs137854469
1 1.000 0.160 15 48485418 missense variant C/A;T snv 0.800 1.000 30 1993 2017
dbSNP: rs137854470
rs137854470
1 1.000 0.160 15 48487425 missense variant C/T snv 0.800 1.000 30 1993 2017
dbSNP: rs137854474
rs137854474
1 1.000 0.160 15 48483863 missense variant A/G snv 0.800 1.000 30 1993 2017
dbSNP: rs137854482
rs137854482
1 1.000 0.160 15 48487389 missense variant C/T snv 0.800 1.000 30 1993 2017
dbSNP: rs363804
rs363804
1 1.000 0.160 15 48441771 missense variant C/T snv 7.0E-06 0.800 1.000 30 1993 2017
dbSNP: rs363815
rs363815
1 1.000 0.160 15 48437370 missense variant A/G snv 0.800 1.000 30 1993 2017
dbSNP: rs111929350
rs111929350
1 1.000 0.160 15 48452603 missense variant C/A;G;T snv 0.800 1.000 12 1996 2017
dbSNP: rs111588631
rs111588631
1 1.000 0.160 15 48428391 missense variant A/G snv 0.800 1.000 10 1996 2017
dbSNP: rs141133182
rs141133182
1 1.000 0.160 15 48415735 stop gained C/A;T snv 2.1E-04 0.800 1.000 10 1996 2017
dbSNP: rs397515771
rs397515771
1 1.000 0.160 15 48495560 missense variant G/C snv 0.700 1.000 7 1998 2014
dbSNP: rs397515790
rs397515790
1 1.000 0.160 15 48487383 missense variant T/C snv 0.700 1.000 6 1995 2014
dbSNP: rs397515775
rs397515775
1 1.000 0.160 15 48495513 missense variant C/T snv 0.700 1.000 5 1999 2007
dbSNP: rs1555394580
rs1555394580
1 1.000 0.160 15 48427755 missense variant C/T snv 0.700 1.000 4 1999 2011
dbSNP: rs397515791
rs397515791
1 1.000 0.160 15 48487362 missense variant C/A;G snv 0.700 1.000 4 1999 2009
dbSNP: rs397515794
rs397515794
1 1.000 0.160 15 48600213 missense variant C/T snv 0.700 1.000 4 1999 2011
dbSNP: rs397515818
rs397515818
1 1.000 0.160 15 48596324 missense variant C/G snv 0.700 1.000 4 1997 2010
dbSNP: rs1566895262
rs1566895262
1 1.000 0.160 15 48434641 missense variant C/A snv 0.700 1.000 3 1999 2016
dbSNP: rs363810
rs363810
1 1.000 0.160 15 48422024 missense variant A/G;T snv 0.700 1.000 3 1999 2005
dbSNP: rs363821
rs363821
1 1.000 0.160 15 48434701 missense variant C/A;T snv 0.700 1.000 3 1999 2006
dbSNP: rs397515755
rs397515755
1 1.000 0.160 15 48520711 stop gained G/T snv 0.700 1.000 3 1999 2014