Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13 4
rs7952436
KDM2A
11 67257063 3 prime UTR variant C/T snv 4.7E-02 3
rs33966734
CCND3
6 41936060 stop gained C/A;G;T snv 1.2E-02; 4.0E-06 2