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: rs28940569
rs28940569
1 1.000 0.120 8 1780495 missense variant G/C snv 0.800 1.000 7 2004 2016
dbSNP: rs386834125
rs386834125
1 1.000 0.120 8 1771281 missense variant A/G snv 0.800 1.000 7 2004 2016
dbSNP: rs386834126
rs386834126
1 1.000 0.120 8 1771374 missense variant T/G snv 0.800 1.000 7 2004 2016
dbSNP: rs386834133
rs386834133
1 1.000 0.120 8 1780287 missense variant A/G snv 0.800 1.000 7 2004 2016
dbSNP: rs386834132
rs386834132
1 1.000 0.120 8 1780265 frameshift variant CT/- delins 0.700 1.000 3 2000 2012
dbSNP: rs1057516582
rs1057516582
1 1.000 0.120 8 1771317 frameshift variant A/- del 0.700 0
dbSNP: rs1057516867
rs1057516867
1 1.000 0.120 8 1771101 frameshift variant T/- del 0.700 0
dbSNP: rs1554448874
rs1554448874
1 1.000 0.120 8 1771056 start lost T/C snv 0.700 0
dbSNP: rs1554448924
rs1554448924
1 1.000 0.120 8 1771104 frameshift variant A/- del 0.700 0
dbSNP: rs1554449028
rs1554449028
1 1.000 0.120 8 1771257 frameshift variant C/- delins 0.700 0
dbSNP: rs1554449047
rs1554449047
1 1.000 0.120 8 1771280 stop gained C/T snv 0.700 0
dbSNP: rs1554449124
rs1554449124
1 1.000 0.120 8 1771360 stop gained G/A snv 0.700 0
dbSNP: rs1554449136
rs1554449136
1 1.000 0.120 8 1771366 stop gained G/A snv 0.700 0
dbSNP: rs1554451484
rs1554451484
1 1.000 0.120 8 1780248 splice acceptor variant A/G snv 0.700 0
dbSNP: rs1554451504
rs1554451504
1 1.000 0.120 8 1780299 frameshift variant T/- delins 0.700 0
dbSNP: rs386834123
rs386834123
1 1.000 0.120 8 1771233 inframe deletion AAG/- delins 0.700 0
dbSNP: rs386834128
rs386834128
1 1.000 0.120 8 1771518 missense variant C/A;T snv 0.700 0
dbSNP: rs386834135
rs386834135
1 1.000 0.120 8 1780339 inframe deletion TGG/- delins 0.700 0
dbSNP: rs386834138
rs386834138
1 1.000 0.120 8 1780472 missense variant C/G snv 0.700 0
dbSNP: rs386834139
rs386834139
1 1.000 0.120 8 1771142 frameshift variant G/- del 0.700 0
dbSNP: rs759830733
rs759830733
1 1.000 0.120 8 1771337 stop gained A/T snv 7.0E-06 0.700 0
dbSNP: rs34238807
rs34238807
1 1.000 0.120 8 1771116 frameshift variant G/-;GG delins 4.0E-06 0.700 0
dbSNP: rs386834129
rs386834129
1 1.000 0.120 8 1771100 missense variant C/A;G;T snv 2.0E-05; 4.0E-06 0.700 1.000 7 2004 2016
dbSNP: rs386834127
rs386834127
1 1.000 0.120 8 1771469 missense variant C/T snv 4.0E-06 0.800 1.000 7 2004 2016
dbSNP: rs746397087
rs746397087
1 1.000 0.120 8 1780469 stop gained C/T snv 4.0E-06 0.700 1.000 2 2000 2017