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: rs587784245
rs587784245
1 1.000 0.080 17 2681734 missense variant C/T snv 0.700 0
dbSNP: rs587784247
rs587784247
1 1.000 0.080 17 2681762 missense variant G/A snv 0.700 0
dbSNP: rs587784248
rs587784248
1 1.000 0.080 17 2681765 missense variant G/C snv 0.700 0
dbSNP: rs587784249
rs587784249
1 1.000 0.080 17 2681770 missense variant G/C snv 0.700 0
dbSNP: rs587784250
rs587784250
1 1.000 0.080 17 2666019 missense variant G/A snv 0.700 0
dbSNP: rs587784251
rs587784251
1 1.000 0.080 17 2681802 stop lost A/C snv 0.700 0
dbSNP: rs587784252
rs587784252
1 1.000 0.080 17 2666031 frameshift variant AA/- delins 0.700 0
dbSNP: rs587784253
rs587784253
1 1.000 0.080 17 2666047 frameshift variant T/- delins 0.700 0
dbSNP: rs587784254
rs587784254
1 1.000 0.080 17 2666061 missense variant T/A snv 0.700 0
dbSNP: rs587784256
rs587784256
1 1.000 0.080 17 2666091 splice donor variant G/A;T snv 4.9E-06 0.700 0
dbSNP: rs587784257
rs587784257
1 1.000 0.080 17 2666090 missense variant G/C snv 0.700 0
dbSNP: rs587784258
rs587784258
1 1.000 0.080 17 2667064 stop gained C/T snv 0.700 0
dbSNP: rs587784259
rs587784259
1 1.000 0.080 17 2667103 stop gained -/A delins 0.700 0
dbSNP: rs587784260
rs587784260
1 1.000 0.080 17 2665369 splice region variant C/G;T snv 0.700 0
dbSNP: rs587784261
rs587784261
1 1.000 0.080 17 2667170 missense variant T/A snv 0.700 0
dbSNP: rs587784262
rs587784262
1 1.000 0.080 17 2665376 stop gained C/A;G;T snv 0.700 0
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