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
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 3
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs10494964
LOC105372912
1 213793544 intron variant T/C snv 0.45 2
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs114948639
PRKCE
2 46066687 intron variant C/T snv 7.2E-03 3
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs11689538
TFCP2L1
2 121238062 intron variant G/C snv 0.11 3
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 3
rs12811512
GPRC5A
12 12893277 intron variant C/T snv 0.11 3
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs12945870
KDM6B ; DNAH2 ; LOC105371516
17 7834013 downstream gene variant C/G;T snv 2
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs149804345 3 56710234 intergenic variant AACAAA/-;AACAAAAACAAA;AACAAAAACAAAAACAAA delins 3
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17287978 6 43973400 intergenic variant T/C snv 3.3E-02 3
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs17773190
LINC01118
2 46803224 intron variant A/G snv 0.32 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs184088518
EGLN2 ; RAB4B-EGLN2
19 40799233 5 prime UTR variant G/T snv 1.8E-02 2
rs1936807
RSPO3
6 127127104 intron variant C/G snv 0.55 4
rs1997595 21 15205839 intron variant A/C;G snv 3