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
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
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
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
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
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
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
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 14