Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs7901695 0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs46522 0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs4773144 0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs7195830 0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs157580 0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33