Disease: Hematocrit procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
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