Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10849020 12 4222843 intergenic variant C/G snv 0.22 3
rs10849023 12 4223312 intergenic variant C/T snv 0.22 4
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs115616389 4 54323915 intergenic variant C/T snv 2.0E-02 2
rs12146644 11 95759714 upstream gene variant A/G snv 0.28 2
rs12196049 6 121464945 intergenic variant A/C snv 0.18 2
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs12453682 17 39613752 upstream gene variant C/G;T snv 2
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs13165424 5 154973452 downstream gene variant A/G snv 0.24 2
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
rs144942726 13 51921254 non coding transcript exon variant C/G;T snv 2.3E-02 2
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
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
rs188778252 4 54182639 intron variant C/G;T snv 2
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs2672092 15 81578279 intron variant T/C snv 0.40 2
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs4663199 2 235459395 regulatory region variant T/A snv 0.35 2
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs5872391 5 154655826 intergenic variant AA/-;A delins 0.35 3