Disease: Mean corpuscular hemoglobin concentration determination
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs2160906
TMPRSS6
22 37097138 intron variant G/A snv 0.17 3
rs228904
TMPRSS6
22 37098774 intron variant A/G snv 0.17 2