Disease: Platelet Count measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
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
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs1059196
SEPT5-GP1BB ; GP1BB
22 19724571 3 prime UTR variant C/T snv 0.42 3
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs117672662
ACTN1
14 68958750 intron variant T/C snv 7.4E-03 3