Disease: Mean Corpuscular Volume (result)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs136211
MYH9
22 36362502 intron variant A/G snv 0.62 2
rs141007801
CASC15
6 21722558 intron variant A/-;AA;AAA;AAAA delins 2
rs148041301 13 40695520 intergenic variant G/A snv 2.9E-02 2
rs149388997
FBXO7
22 32498965 downstream gene variant GTTTT/-;GTTTTGTTTT delins 0.41 2
rs149514089 6 16167286 upstream gene variant C/T snv 2.0E-03 2
rs150658949
MIPOL1
14 37218925 intron variant AAAAAAAAA/-;A;AA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAAA delins 2
rs150854910
TF
3 133757925 missense variant C/T snv 8.4E-04 9.4E-04 2
rs1578741 1 117716081 intergenic variant A/C snv 0.19 2
rs16895130
CCND3
6 41957193 intron variant A/G snv 0.22 2
rs17348614
NPHP3-ACAD11 ; NPHP3
3 132692324 intron variant C/T snv 4.4E-02 2
rs17700466 7 93006659 regulatory region variant A/C snv 0.12 2
rs17720193
NCOA4
10 46017981 intron variant A/G snv 2.5E-02 2
rs17803780
RCL1 ; MIR101-2
9 4849647 intron variant T/C snv 0.19 2
rs181743661
INTU
4 127647811 intron variant C/T snv 8.5E-03 2
rs200510190
CNNM2
10 103031838 intron variant C/- del 0.41 2
rs2140875 7 129963039 intron variant A/G snv 0.80 2
rs2290707
RRM2B ; UBR5-AS1
8 102239027 upstream gene variant C/A snv 2.8E-02 2
rs239260
SLC22A20P
11 65216232 intron variant G/A snv 0.64 2
rs2572207
DENND4A ; RAB11A
15 65778355 intron variant C/A;T snv 2
rs2696579
KANSL1
17 46150027 intron variant T/A;C snv 2
rs2713936
TEX9
15 56253787 intron variant A/C snv 0.32 2
rs2836422
ERG
21 38466112 intron variant T/A snv 0.46 2
rs28874975 22 32506416 downstream gene variant G/A;T snv 2
rs2974760
HBZ
16 152050 intron variant C/A snv 0.58 2
rs33964027
EXOSC9
4 121808259 intron variant TTAC/- delins 0.31 2