Disease: Hematocrit procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs60695258
AFF1
4 87101557 intron variant C/A;T snv 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9