Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs5987027
MPP1
X 154785832 intron variant C/T snv 7.8E-02 2
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs4823308
LINC01589
22 45604058 downstream gene variant T/A snv 0.38 3
rs5762813
ZNRF3
22 28807326 intron variant C/T snv 0.25 3
rs9330813
WNT7B
1.000 0.040 22 45968281 intron variant G/A;C snv 3
rs2251655
TMPRSS6
22 37094652 intron variant C/T snv 0.42 2
rs470119
TYMP
22 50528485 non coding transcript exon variant T/C;G snv 0.61; 8.2E-06 2
rs5756825
H1-0
22 37803943 upstream gene variant T/C snv 0.58 2
rs7287312 22 50649753 intergenic variant T/A snv 3.3E-02 2
rs9697691 22 45914013 intergenic variant C/G snv 0.43 2
rs11914181
MAFF ; PLA2G6
22 38206133 intron variant T/C snv 0.56 1
rs13058451
BCL2L13
22 17685093 intron variant T/C;G snv 1
rs131780
LOC105373098 ; KLHDC7B
22 50544110 upstream gene variant C/A;G snv 0.20 1
rs139380
CBX7
22 39130169 intron variant T/C snv 0.70 1
rs171277 22 21902186 intergenic variant A/G snv 0.49 1
rs179468
CHCHD10 ; LOC107985577
22 23767587 synonymous variant T/G snv 0.81 0.92 1
rs2072860
TMPRSS6
22 37074564 intron variant G/A snv 0.53 0.59 1
rs5753627
DRG1 ; EIF4ENIF1
22 31463873 synonymous variant A/G snv 0.10 6.8E-02 1
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 1
rs5756506
TMPRSS6
22 37071352 intron variant G/A;C snv 1
rs5765524
FBLN1
22 45596337 intron variant A/G snv 0.36 1
rs5998517 22 32503058 downstream gene variant T/C snv 0.55 1
rs66781836
A4GALT
22 42719514 intron variant TTCT/-;TTCTTTCT delins 1