Disease: Hematocrit procedure
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 9
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5