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
rs10494964
LOC105372912
1 213793544 intron variant T/C snv 0.45 2
rs12945870
KDM6B ; DNAH2 ; LOC105371516
17 7834013 downstream gene variant C/G;T snv 2
rs184088518
EGLN2 ; RAB4B-EGLN2
19 40799233 5 prime UTR variant G/T snv 1.8E-02 2
rs2923411 8 42600063 intergenic variant T/C snv 0.66 2
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 3
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
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
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 3
rs12811512
GPRC5A
12 12893277 intron variant C/T snv 0.11 3
rs149804345 3 56710234 intergenic variant AACAAA/-;AACAAAAACAAA;AACAAAAACAAAAACAAA delins 3
rs17287978 6 43973400 intergenic variant T/C snv 3.3E-02 3
rs17773190
LINC01118
2 46803224 intron variant A/G snv 0.32 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs2269188
SIM2 ; LOC107985492 ; LOC105369308
21 36700056 intron variant G/C snv 0.24 3
rs2732480
ZNF641
12 48342520 3 prime UTR variant C/A snv 0.39 3
rs35060063 3 194956076 intergenic variant G/A snv 0.36 3
rs35542019
LINC00649 ; LOC101928126
21 33974555 non coding transcript exon variant AA/-;A delins 0.57 3
rs366684
PROX1
1 214013919 intron variant G/A;C snv 3
rs3847858 12 51924594 downstream gene variant A/T snv 8.9E-02 3
rs4760682
PFKM
12 48118502 missense variant C/A snv 0.85 0.87 3
rs4823308
LINC01589
22 45604058 downstream gene variant T/A snv 0.38 3
rs533281866
EGLN1
1 231422308 intron variant G/A;C snv 3
rs56262900
KLHL29
2 23674855 intron variant G/A snv 7.6E-02 3