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: rs587784263
rs587784263
1 1.000 0.080 17 2667185 missense variant A/T snv 0.700 0
dbSNP: rs587784264
rs587784264
1 1.000 0.080 17 2667199 splice donor variant G/A snv 0.700 0
dbSNP: rs587784265
rs587784265
1 1.000 0.080 17 2638291 start lost G/A snv 0.700 0
dbSNP: rs587784266
rs587784266
1 1.000 0.080 17 2670168 stop gained G/A snv 0.700 0
dbSNP: rs587784267
rs587784267
1 1.000 0.080 17 2670193 stop gained C/T snv 0.700 0
dbSNP: rs587784268
rs587784268
1 1.000 0.080 17 2670216 frameshift variant CT/- delins 0.700 0
dbSNP: rs587784269
rs587784269
1 1.000 0.080 17 2670223 stop gained C/T snv 0.700 0
dbSNP: rs587784270
rs587784270
1 1.000 0.080 17 2670285 frameshift variant AACTA/- delins 0.700 0
dbSNP: rs587784271
rs587784271
1 1.000 0.080 17 2670297 frameshift variant T/-;TT delins 0.700 0
dbSNP: rs587784272
rs587784272
1 1.000 0.080 17 2665395 missense variant T/G snv 0.700 0
dbSNP: rs587784273
rs587784273
1 1.000 0.080 17 2672718 stop gained C/G snv 0.700 0
dbSNP: rs587784274
rs587784274
1 1.000 0.080 17 2672724 frameshift variant CTATAAAA/- delins 0.700 0
dbSNP: rs587784275
rs587784275
1 1.000 0.080 17 2672731 frameshift variant TA/- delins 0.700 0
dbSNP: rs587784276
rs587784276
1 1.000 0.080 17 2672743 stop gained G/A;T snv 4.0E-06 0.700 0
dbSNP: rs587784277
rs587784277
1 1.000 0.080 17 2672742 frameshift variant G/- delins 0.700 0
dbSNP: rs587784278
rs587784278
1 1.000 0.080 17 2672750 stop gained C/T snv 0.700 0
dbSNP: rs587784279
rs587784279
1 1.000 0.080 17 2672761 splice region variant A/G snv 0.700 0
dbSNP: rs587784280
rs587784280
1 1.000 0.080 17 2672762 splice region variant G/A snv 0.700 0
dbSNP: rs587784281
rs587784281
1 1.000 0.080 17 2672757 missense variant G/A snv 1.2E-05 0.700 0
dbSNP: rs587784282
rs587784282
1 1.000 0.080 17 2674063 stop gained C/G;T snv 4.0E-06 0.700 0
dbSNP: rs587784284
rs587784284
1 1.000 0.080 17 2674103 frameshift variant -/T delins 0.700 0
dbSNP: rs587784285
rs587784285
1 1.000 0.080 17 2665411 stop gained T/G snv 0.700 0
dbSNP: rs587784286
rs587784286
1 1.000 0.080 17 2674118 stop gained C/T snv 0.700 0
dbSNP: rs587784287
rs587784287
1 1.000 0.080 17 2674139 missense variant A/C snv 0.700 0
dbSNP: rs587784288
rs587784288
1 1.000 0.080 17 2674229 missense variant T/C snv 0.700 0