Disease: Corpuscular Hemoglobin Concentration Mean
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
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
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 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
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 4
rs117747069
NPRL3
16 120077 intron variant G/C snv 2.5E-02 4
rs11864973
HBZ
16 143225 intron variant G/A;T snv 3.6E-02 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4