Disease: Corpuscular Hemoglobin Concentration Mean
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs2418736
NFATC3
16 68120959 intron variant G/A snv 0.28 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs1109166
LCAT ; SLC12A4
16 67943479 5 prime UTR variant T/C snv 0.32 3
rs12449157
GFOD2
1.000 0.040 16 67674994 3 prime UTR variant A/G snv 0.30 3
rs20549
PSMB10
16 67936027 missense variant A/G;T snv 0.22 0.31 3
rs3743739
PLA2G15
16 68259417 synonymous variant T/C snv 0.19 0.22 3
rs4129767
PGS1
17 78407903 intron variant G/A snv 0.46 3
rs7187202 16 68239992 upstream gene variant T/C snv 0.21 3
rs8048034
NFATC3
16 68176701 intron variant A/G snv 0.23 3