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
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 3
rs11789898
BRD3
9 134060541 intron variant G/T snv 0.14 2
rs12637184
ACTRT3
3 169769649 non coding transcript exon variant G/A snv 0.20 2
rs2958137
HSD17B6
12 56757545 intron variant A/C;G;T snv 2