Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 5
rs1172129
TMCC2
1 205275844 intron variant T/A snv 0.30 2
rs1172130
TMCC2
1 205275825 intron variant G/A snv 0.30 2
rs13120301
AFF1
4 87065243 intron variant C/T snv 0.39 2
rs1668873
TMCC2
1 205266862 intron variant G/A snv 0.27 2
rs9660992
TMCC2
1 205280322 intron variant A/G snv 0.43 2