Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008084
CCDC162P
6 109305762 intron variant G/A snv 0.40 3
rs10736831
TMEM72-AS1
10 44906863 intron variant G/A snv 0.55 3
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs10758658
RCL1
9 4856877 intron variant G/A snv 0.15 4
rs10793565
TMEM72-AS1
10 44892783 intron variant G/C snv 0.53 3
rs11085825
GCDH
19 12896644 intron variant C/T snv 0.31 3
rs1122794
FAM234A
16 259156 intron variant C/A snv 0.19 2
rs11239550
MARCHF8
10 45529281 intron variant A/G snv 0.31 3
rs11248850
NPRL3
16 113599 intron variant G/A snv 0.38 2
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs117747069
NPRL3
16 120077 intron variant G/C snv 2.5E-02 4
rs11811522
SPTA1
1 158634353 intron variant G/A snv 0.35 2
rs11857609
LOC105370866 ; RAB11A
15 65802932 intron variant T/C snv 0.68 3
rs11864973
HBZ
16 143225 intron variant G/A;T snv 3.6E-02 4
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs12530845
NUP205
7 135645230 intron variant T/C snv 0.21 2
rs12532878
MOSPD3
7 100614631 intron variant G/A;C snv 0.18 2
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
rs131777
SYCE3
22 50552604 intron variant C/T snv 0.63 3
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
rs1408272
SLC17A3
6 25842723 intron variant T/G snv 4.0E-02 4