Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710
MAGEL2
0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs104893755
POU1F1
0.851 0.200 3 87259959 missense variant G/A snv 5
rs121917843
PROP1
0.882 0.160 5 177994231 missense variant G/A snv 4.0E-06 3
rs201781653
BRD2
0.925 0.080 6 32977805 missense variant C/A;T snv 4.1E-06; 1.6E-05 2
rs28936416
HESX1
0.925 0.120 3 57199842 missense variant A/G snv 2
rs768165720
HESX1
0.925 0.120 3 57198784 missense variant C/T snv 7.6E-05 1.1E-04 2
rs199761861
OTX2
0.925 0.080 14 56802204 missense variant G/C;T snv 2.1E-04; 1.6E-05 2
rs104893766
POU1F1
0.925 0.160 3 87262138 missense variant G/C snv 2
rs772390221
POU1F1
0.925 0.160 3 87261296 frameshift variant CTTTC/- delins 2
rs780359925
POU1F1
0.925 0.160 3 87259977 missense variant G/A snv 8.0E-06 2
rs121917839
PROP1
0.925 0.120 5 177993032 missense variant G/A snv 6.8E-05 4.9E-05 2
rs121917841
PROP1
0.925 0.120 5 177994185 missense variant A/G snv 2
rs137853100
PROP1
0.925 0.120 5 177994152 missense variant C/T snv 3.6E-05 2.1E-05 2
rs1292127844
HESX1
1.000 0.080 3 57198449 missense variant C/G snv 4.0E-06 1
rs1465556147
HESX1
1.000 0.080 3 57198805 missense variant T/C snv 7.0E-06 1
rs766234350
HESX1
1.000 0.080 3 57198276 missense variant C/T snv 8.0E-06 2.8E-05 1
rs770886420
HESX1
1.000 0.080 3 57198280 missense variant G/A snv 2.0E-05 3.5E-05 1
rs1169159883
HNF1A
1.000 0.080 12 120994164 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs142400016
LHX3
1.000 0.080 9 136200631 missense variant G/A snv 4.8E-05 6.3E-05 1
rs777331392
LHX3
1.000 0.080 9 136199032 missense variant C/A;T snv 1
rs779490520
LHX4
1.000 0.080 1 180266520 missense variant C/T snv 1.2E-05 7.0E-06 1
rs1318234609
PDLIM5
1.000 0.080 4 94579531 missense variant T/C snv 1.4E-05 1
rs1237859972
POMC
1.000 0.080 2 25161178 missense variant C/T snv 1