Disease: Mean Corpuscular Volume (result)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10420951 19 18526808 upstream gene variant C/G snv 0.81 2
rs10849023 12 4223312 intergenic variant C/T snv 0.22 4
rs10923397 1 117708521 regulatory region variant C/T snv 0.14 2
rs11031096 11 4139451 upstream gene variant T/C snv 0.47 2
rs11611397 12 4222106 intergenic variant G/T snv 0.22 2
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs12563213 1 154318779 upstream gene variant G/C snv 0.30 2
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 5
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs148041301 13 40695520 intergenic variant G/A snv 2.9E-02 2
rs149514089 6 16167286 upstream gene variant C/T snv 2.0E-03 2
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
rs1578741 1 117716081 intergenic variant A/C snv 0.19 2
rs169219 6 25957164 intergenic variant C/A;G snv 3
rs17064262 6 135144336 intergenic variant T/C snv 0.18 4
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs17700466 7 93006659 regulatory region variant A/C snv 0.12 2
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs2140875 7 129963039 intron variant A/G snv 0.80 2
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs28874975 22 32506416 downstream gene variant G/A;T snv 2