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
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs12196049 6 121464945 intergenic variant A/C snv 0.18 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs2224797
LMO7-AS1 ; LMO7
13 75636606 5 prime UTR variant A/C snv 0.50 2
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs9357371
MED20
6 41917581 5 prime UTR variant A/C snv 0.20 4
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 4
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs6568571
CCDC162P
6 109292049 intron variant A/C;T snv 3
rs741702
GCDH ; SYCE2
19 12913436 intron variant A/C;T snv 3
rs1010222
CALR
19 12937794 upstream gene variant A/G snv 0.70 3
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 4
rs11211480
TAL1
1 47227548 non coding transcript exon variant A/G snv 0.42 4
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs12146644 11 95759714 upstream gene variant A/G snv 0.28 2
rs13165424 5 154973452 downstream gene variant A/G snv 0.24 2
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
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
rs1421312
TMPRSS6
22 37091770 intron variant A/G snv 0.45 4