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
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
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
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
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
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
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 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
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4