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
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs11072566
NRG4
0.925 0.120 15 76001630 intron variant A/G snv 0.45 5
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5
rs218264 4 54542708 intergenic variant A/G;T snv 5