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
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 4
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs12636078
KAT2B
3 20064181 intron variant A/G;T snv 3
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 5
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs13220662
HBS1L
6 135074410 intron variant G/A snv 0.41 4
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs140429100
PDAP1
7 99397842 intron variant G/A snv 1.5E-02 1.6E-02 2
rs1421312
TMPRSS6
22 37091770 intron variant A/G snv 0.45 4
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs148125759
UGCG
9 111901105 intron variant T/C snv 1.0E-02 4
rs148910659
KANSL1
17 46055293 intron variant G/A snv 3
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs151305716
ZNF217
20 53605567 intron variant C/T snv 8.1E-03 3
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs16928078
C11orf21 ; TSPAN32
11 2298783 intron variant C/T snv 0.15 4
rs17116384
ZBTB16
11 114110519 intron variant A/G snv 0.25 3
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8