Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 1
rs11107
FBXO7
1.000 0.040 22 32479203 start lost G/A;C snv 0.45; 8.0E-06 1
rs2235324
TMPRSS6
22 37089684 missense variant T/C snv 0.38 0.40 3
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 2
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs2246434
SPTA1
1 158648665 intron variant G/A snv 0.26 0.22 2
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 3
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 1
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 1
rs9924561
FAM234A
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 1
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 1
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 2
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12