Source: GWASDB ×
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 14
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 2