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
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs112257498
SLC40A1
2 189568259 intron variant C/G;T snv 2
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 4
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12453682 17 39613752 upstream gene variant C/G;T snv 2
rs12636078
KAT2B
3 20064181 intron variant A/G;T snv 3
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 5
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs148910659
KANSL1
17 46055293 intron variant G/A snv 3
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs188778252 4 54182639 intron variant C/G;T snv 2
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs2556097
LY75 ; LY75-CD302
2 159830550 intron variant C/A;T snv 2
rs2661794
SPRED2
2 65412409 intron variant C/A;T snv 2
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs3743879
RGS11 ; FAM234A
16 268475 3 prime UTR variant C/A;G snv 2
rs42042
CDK6
7 92617798 intron variant C/A;G;T snv 2
rs470119
TYMP
22 50528485 non coding transcript exon variant T/C;G snv 0.61; 8.2E-06 4
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 14
rs496321
LOC101929295
11 95153468 intron variant T/C;G snv 3