Disease: Platelet Count measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 2
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 3
rs12096438
LDLRAP1
1 25562931 non coding transcript exon variant C/A;T snv 2
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs41315846
GCSAML
1 247549001 intron variant T/C snv 0.44 0.52 3
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs17572109
ARPC2
2 218229211 non coding transcript exon variant G/A;T snv 3
rs655029
EHD3
2 31254972 intron variant G/A snv 0.78 3
rs7585866 2 191831529 downstream gene variant A/G snv 0.24 2
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs17825630
ARHGEF3
3 56916027 intron variant G/A snv 0.12 2
rs3804749
PDIA5
3 123114156 intron variant C/T snv 0.48 3
rs7641175
TBC1D5
3 18269920 intron variant G/A snv 0.81 3
rs4699154 4 105112927 intron variant T/A;C snv 2
rs10940072
MAST4
5 66620956 intron variant G/A snv 0.37 2
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 4
rs34950321
IQGAP2
5 76668682 missense variant C/T snv 1.7E-02 1.6E-02 3
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3778028
ETV7
6 36381889 intron variant C/A snv 7.2E-02 2
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 3
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9