Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs2232365 0.716 0.480 X 49259429 intron variant T/C snv 16
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs12917707 0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs4819554 0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2576178 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9