Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs762471803 0.925 0.040 11 102114201 missense variant T/G snv 6
rs761872690 0.925 0.080 11 101128246 synonymous variant G/A snv 2.8E-05 3
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs759478535 0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs759435862 0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs756160717 3 12585204 missense variant G/A snv 1.2E-05 2.1E-05 1
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 7
rs754854286 1.000 0.120 10 31520432 missense variant G/C snv 3
rs753066745 X 81277164 missense variant C/T snv 1.7E-05 9.5E-06 2
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs746429 0.882 0.120 11 65649963 synonymous variant G/A snv 0.31 0.30 8
rs7371084 0.925 0.120 2 48712814 intron variant T/C snv 0.12 3
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs730882002 0.925 0.040 17 7674956 missense variant T/C snv 6
rs723526 1.000 7 55067126 intron variant A/G snv 0.86 2
rs71310379 3 179199003 missense variant C/A snv 4.4E-05 4.2E-05 1
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs7034162 0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs6983561 0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs6973569 0.851 0.080 7 34583412 intron variant G/A snv 4.7E-02 5