Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10964862 9 21151554 intergenic variant C/A;G snv 1
rs946486 9 130770618 intron variant C/T snv 0.44 1
rs867748453 7 140781608 missense variant G/A snv 1
rs353630 1.000 0.080 11 35166644 intron variant G/A snv 0.33 1
rs3206652 3 108046402 3 prime UTR variant T/C snv 0.27 1
rs3804639 3 108071988 intron variant G/T snv 0.28 1
rs9879947 3 108046545 3 prime UTR variant G/A snv 0.45 1
rs684559 1 111215824 intron variant G/A snv 0.27 1
rs1053129 5 80626901 3 prime UTR variant C/A;T snv 1
rs1472189 11 11962338 3 prime UTR variant C/T snv 0.25 1
rs7795743 7 55182437 non coding transcript exon variant G/A snv 0.56 1
rs1131692237 1.000 0.040 17 39725161 missense variant T/G snv 1
rs10964859 9 21140673 3 prime UTR variant C/A;G snv 1
rs779724499 12 54411885 missense variant G/A snv 1
rs200246209 11 102527789 synonymous variant G/A snv 8.0E-06 1.4E-05 1
rs2375801 4 186550471 intron variant T/C snv 0.34 1
rs370006648
NDN
15 23687168 missense variant G/A snv 4.1E-05 7.0E-05 1
rs148626207 4 102612593 missense variant T/C snv 8.0E-06 1.4E-05 1
rs71310379 3 179199003 missense variant C/A snv 4.4E-05 4.2E-05 1
rs756160717 3 12585204 missense variant G/A snv 1.2E-05 2.1E-05 1
rs2994809 1 119809354 intron variant T/C snv 0.91 1
rs377767422
RET
10 43119635 missense variant C/T snv 1.2E-05 2.1E-05 1
rs1317052311 X 15358134 missense variant C/A snv 5.5E-06 1
rs6475526 1.000 0.080 9 21242162 upstream gene variant C/T snv 0.33 2
rs1340026226
AR
1.000 0.080 X 67711662 missense variant G/A snv 9.5E-06 2