Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs314253
DLG4
17 7188331 downstream gene variant T/C snv 0.37 3
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 3
rs1880889
PDZRN4
12 41327433 intron variant A/C snv 0.91 2
rs2445752
CYP19A1 ; MIR4713HG
15 51284188 intron variant A/G snv 0.30 2
rs6911965
GPLD1
6 24480067 intron variant T/A;C snv 2
rs8176720
ABO
9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 2
rs9533090
LINC02341
13 42377313 intron variant C/T snv 0.39 2
rs10091910
NCOA2
8 70196313 intron variant T/A;C snv 1
rs10761779
JMJD1C
10 63515167 intron variant A/G snv 0.42 1
rs10819937 9 101460951 intergenic variant C/G;T snv 1
rs10822161
JMJD1C
10 63358443 intron variant G/A;T snv 1
rs11573824
TNFRSF11B
8 118947686 intron variant A/C;T snv 0.67 1
rs117047270
SLC26A4
7 107664388 intron variant T/A snv 3.3E-03 1
rs117298830
PGGHG
11 291521 non coding transcript exon variant A/T snv 3.0E-03 1
rs12197384
KIAA0319
6 24549087 intron variant C/T snv 7.5E-02 1
rs12277152
PGGHG
11 296255 downstream gene variant G/A;C snv 1
rs12355784
JMJD1C
10 63361805 intron variant C/A;T snv 1
rs138612106
GPLD1
6 24427826 3 prime UTR variant A/G snv 0.17 1
rs139089160
CDA
1 20592062 intron variant G/A;T snv 1
rs143370804
EIF4G3
1 21024072 intron variant G/A snv 0.34 1
rs144391488
BTNL2 ; TSBP1-AS1
6 32400783 intron variant C/G;T snv 1
rs150674717
ALDH5A1
6 24512970 intron variant G/A snv 2.0E-04 1
rs16856332
ABCB11
2 168984064 intron variant T/A;G snv 1
rs17300770
GPLD1
6 24462792 missense variant G/C snv 0.12 0.10 1