Disease: Hematocrit procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs4666014
RBKS ; MRPL33
2 27796308 intron variant G/A snv 0.36 2
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16