Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894972
SRY
0.807 0.240 Y 2787320 missense variant C/T snv 6
rs104894966
SRY
0.882 0.200 Y 2787267 missense variant C/T snv 3
rs104894971
SRY
0.882 0.200 Y 2787551 missense variant C/T snv 4.4E-05 3
rs104894959
SRY
0.925 0.160 Y 2787334 missense variant G/C snv 1.5E-05 2
rs104894974
SRY
0.925 0.160 Y 2787321 missense variant C/G snv 2
rs1556370543
SRY
0.925 0.160 Y 2787273 stop gained G/A snv 2
rs104894956
SRY
1.000 0.160 Y 2787278 missense variant A/G snv 1
rs104894957
SRY
1.000 0.160 Y 2787426 missense variant C/G snv 1
rs104894958
SRY
1.000 0.160 Y 2787327 stop gained G/A snv 1
rs104894964
SRY
1.000 0.160 Y 2787287 missense variant T/A snv 1
rs104894965
SRY
1.000 0.160 Y 2787395 stop gained C/T snv 1
rs104894967
SRY
1.000 0.160 Y 2787284 stop gained C/T snv 1
rs104894968
SRY
1.000 0.160 Y 2787401 missense variant A/G snv 1
rs104894969
SRY
1.000 0.160 Y 2787412 missense variant C/T snv 1
rs104894970
SRY
1.000 0.160 Y 2787330 stop gained T/A snv 1
rs104894973
SRY
1.000 0.160 Y 2787224 missense variant T/A;C snv 1
rs104894975
SRY
1.000 0.160 Y 2787592 stop gained A/T snv 1
rs104894976
SRY
1.000 0.160 Y 2787207 missense variant G/A snv 1
rs104894977
SRY
1.000 0.160 Y 2787600 stop gained G/A snv 1
rs1057519627
SRY
1.000 0.160 Y 2787377 missense variant C/A snv 1
rs1556370548
SRY
1.000 0.160 Y 2787316 stop gained G/C snv 1
rs1556370556
SRY
1.000 0.160 Y 2787339 frameshift variant -/T delins 1
rs1556370558
SRY
1.000 0.160 Y 2787341 stop gained G/T snv 1
rs1556370576
SRY
1.000 0.160 Y 2787515 missense variant C/A snv 1
rs606231178
SRY
1.000 0.160 Y 2787237 frameshift variant CTCT/- delins 1