Disease: Mean Corpuscular Volume (result)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54 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
rs10420951 19 18526808 upstream gene variant C/G snv 0.81 2
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
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs10783487
ATG101
12 52068035 upstream gene variant G/A;T snv 2
rs10849023 12 4223312 intergenic variant C/T snv 0.22 4
rs10923397 1 117708521 regulatory region variant C/T snv 0.14 2
rs11031096 11 4139451 upstream gene variant T/C snv 0.47 2
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 4
rs111775488
LUC7L
16 192899 intron variant G/C snv 5.8E-02 7.0E-02 2
rs112190912
HBZ
16 146470 intron variant A/G snv 4.7E-02 2
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs1123339
KAT7 ; FAM117A
17 49789170 non coding transcript exon variant G/A snv 6.6E-02 2
rs11239537
LOC105378286 ; MARCHF8
10 45487060 intron variant T/C snv 0.33 2
rs11239550
MARCHF8
10 45529281 intron variant A/G snv 0.31 3
rs1134634
CC2D2A
4 15601446 3 prime UTR variant G/C;T snv 0.58; 9.4E-06 2
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs114056237
MED20
6 41909933 intron variant G/A snv 8.6E-03 2
rs11611397 12 4222106 intergenic variant G/T snv 0.22 2