Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11758688
HCG20
1.000 6 30790571 intron variant C/T snv 0.35 4
rs12122100
LOC728989 ; NBPF13P
1.000 1 147037378 intron variant T/C snv 0.76 4
rs12185555 1.000 2 226694601 regulatory region variant A/G snv 0.25 4
rs12190030
HCG21 ; SFTA2 ; MUCL3
1.000 6 30953587 3 prime UTR variant C/T snv 0.21 4
rs12207756
PSORS1C1 ; CDSN
1.000 6 31118905 intron variant C/T snv 0.14 4
rs12274302
DISC1FP1
1.000 11 90853732 non coding transcript exon variant C/A;G;T snv 4
rs12526481
HCG20
1.000 6 30778856 intron variant C/A snv 0.33 4
rs12527415
HCG20
1.000 6 30786763 intron variant C/T snv 0.35 4
rs12697941
SFTA2 ; MUCL3
1.000 6 30936937 intron variant G/A snv 0.18 4
rs130072
CCHCR1
1.000 6 31144707 missense variant C/T snv 0.10 8.4E-02 4
rs13191519
HLA-B ; LOC112267902 ; LINC02571
1.000 6 31297975 intron variant T/C snv 0.12 4
rs13198118
LINC00243
1.000 6 30802955 intron variant T/G snv 0.17 4
rs13198903 1.000 6 31376380 upstream gene variant C/T snv 6.3E-02 4
rs13201769
HCG20
1.000 6 30788289 intron variant G/A snv 0.35 4
rs13207315
HLA-B ; HLA-C
1.000 6 31273350 intron variant T/C snv 0.13 4
rs13210132
MUC22
1.000 6 31033366 intron variant A/G snv 4.3E-02 4
rs13216197
HLA-B ; LINC02571 ; LOC112267902
1.000 6 31303241 intron variant T/C snv 0.15 4
rs13220225
HCG20
1.000 6 30780025 intron variant G/A snv 0.16 4
rs16897900
HCG20
1.000 6 30788116 intron variant C/A snv 0.35 4
rs16898614
HCG22
1.000 6 31056063 non coding transcript exon variant A/G snv 6.7E-02 4
rs16899205
HLA-B ; LOC112267902 ; LINC02571
1.000 6 31298584 intron variant A/G snv 0.34 4
rs16899207
LINC02571 ; HLA-B ; LOC112267902
1.000 6 31298610 intron variant A/G snv 0.34 4
rs16914280
GRM5
1.000 11 88588556 intron variant C/T snv 4.7E-02 4
rs16948255 1.000 16 74847922 downstream gene variant C/T snv 3.9E-02 4
rs17207190 1.000 6 31601743 intergenic variant G/A;T snv 2.8E-02 4