Disease: Hematocrit procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4666014
RBKS ; MRPL33
2 27796308 intron variant G/A snv 0.36 2
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 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
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24