Disease: Hematocrit procedure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs60695258
AFF1
4 87101557 intron variant C/A;T snv 4