Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10091910
NCOA2
8 70196313 intron variant T/A;C snv 1
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 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
rs10893506
ST3GAL4
0.882 0.080 11 126406065 5 prime UTR variant T/A;C snv 6.4E-06; 0.41 1
rs11216930
PHLDB1
1.000 0.040 11 118618067 intron variant A/C snv 0.22 1
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 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
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs17689159
LINC01229 ; LOC105371356
16 79708493 intron variant T/C snv 0.29 1
rs1780324 1 21495264 intergenic variant A/G snv 0.48 1
rs1827293
NBPF3
1 21468895 missense variant A/G snv 0.53 0.45 1