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
rs1007934
ZFYVE1
14 72996771 intron variant G/A snv 0.33 3
rs1008084
CCDC162P
6 109305762 intron variant G/A snv 0.40 3
rs1010222
CALR
19 12937794 upstream gene variant A/G snv 0.70 3
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54 3
rs10160596
EHBP1L1
11 65583893 non coding transcript exon variant G/A snv 0.20 3
rs10197140
ACOXL
2 110852366 intron variant T/C snv 0.28 3
rs10415135
ZBTB7A
19 4061546 intron variant C/T snv 0.23 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
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs10793565
TMEM72-AS1
10 44892783 intron variant G/C snv 0.53 3
rs10849020 12 4222843 intergenic variant C/G snv 0.22 3
rs10849023 12 4223312 intergenic variant C/T snv 0.22 4
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs10974716
SPATA6L ; PLPP6
9 4661574 intron variant C/G snv 0.20 2
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 4
rs11085825
GCDH
19 12896644 intron variant C/T snv 0.31 3
rs11158716
RAD51B
14 68026441 intron variant G/A snv 0.17 2
rs11211480
TAL1
1 47227548 non coding transcript exon variant A/G snv 0.42 4
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs112257498
SLC40A1
2 189568259 intron variant C/G;T snv 2
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs11338569
ANP32B
9 98001175 intron variant T/-;TT delins 0.25 2
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4