Disease: Mean Corpuscular Volume (result)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 4
rs7085433
TIMM23
1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 4
rs837763
LOC107984842
16 88787321 upstream gene variant C/G;T snv 4
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 3