Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs3812049
SLC12A2 ; LINC01184
5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs41313381
ADGRL4
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05 4
rs586178
RHCE
1 25420739 missense variant G/A;C snv 8.4E-05; 0.41 4
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs8176644
ABO
9 133273734 intron variant C/T snv 4
rs113635136
TFRC
3 196075973 intron variant AA/-;A;AAA;AAAA delins 3
rs11456863 3 12230419 regulatory region variant T/-;TT;TTT;TTTTTTTTTTT delins 3
rs12151021
ABCA7
19 1050875 intron variant A/G;T snv 0.69 3
rs2468024
MTDH
8 97652425 intron variant G/A;C snv 3
rs2761436 1 207746403 intergenic variant C/A;T snv 3
rs2901656
C1orf105
1 172465672 3 prime UTR variant C/A;T snv 0.51 3
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 3
rs428073
TAOK3
1.000 0.080 12 118244946 missense variant C/G;T snv 0.72 3
rs4619875
TIGD4 ; ARFIP1
4 152779978 5 prime UTR variant C/G;T snv 3
rs4976033 5 68418419 regulatory region variant A/C;G;T snv 3
rs6084653
SMOX
20 4176425 intron variant C/G;T snv 3
rs6119267
NOL4L-DT ; NOL4L
20 32576112 intron variant C/A;G snv 3
rs61387190
SMG9
19 43756777 upstream gene variant C/A;T snv 3
rs6150565
ANK1
8 41655063 3 prime UTR variant AGAGTCTATACAGC/-;AGAGTCTATACAGCAGAGTCTATACAGC delins 3
rs61750929 9 88880220 regulatory region variant C/A;T snv 3
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs79674254
AK9
6 109501078 intron variant C/A;T snv 3
rs9314323
BNIP3L
8 26385620 intron variant A/G;T snv 3