Disease: Red Blood Cell Count measurement
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
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
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
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
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
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
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 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
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5