Disease: Platelet Count measurement
Source: ALL
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 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4