Disease: Platelet 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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
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
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs34950321
IQGAP2
5 76668682 missense variant C/T snv 1.7E-02 1.6E-02 3
rs8073060
SLFN14 ; LOC107985032
17 35548243 missense variant T/A snv 0.32 0.34 3