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
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 4
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs149290349
ZFP36L2
2 43224818 missense variant G/A;T snv 6.7E-02 3
rs2284344
TNFRSF1A
12 6336163 intron variant G/C snv 0.49 2
rs34038797
NINJ2-AS1 ; NINJ2
12 630843 intron variant C/G snv 0.42 2