Disease: Mean Corpuscular Volume (result)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10783487
ATG101
12 52068035 upstream gene variant G/A;T snv 2
rs1134634
CC2D2A
4 15601446 3 prime UTR variant G/C;T snv 0.58; 9.4E-06 2
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs11669479
HDGFL2
19 4485049 intron variant A/G;T snv 2
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs1203039
RAB11FIP3
16 461337 intron variant G/A;C snv 2
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 4
rs12232375
ZFPM1
16 88500003 intron variant G/A;C;T snv 2
rs12636078
KAT2B
3 20064181 intron variant A/G;T snv 3
rs13091206
CCDC36
3 49201285 intron variant A/C;G snv 2
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
rs141007801
CASC15
6 21722558 intron variant A/-;AA;AAA;AAAA delins 2
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4
rs148910659
KANSL1
17 46055293 intron variant G/A snv 3
rs150658949
MIPOL1
14 37218925 intron variant AAAAAAAAA/-;A;AA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAAA delins 2
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs169219 6 25957164 intergenic variant C/A;G snv 3
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs2572207
DENND4A ; RAB11A
15 65778355 intron variant C/A;T snv 3
rs2696579
KANSL1
17 46150027 intron variant T/A;C snv 2
rs28874975 22 32506416 downstream gene variant G/A;T snv 2
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5