Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 2
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs10484092
FRMD6-AS2 ; FRMD6
1.000 0.040 14 51489516 intron variant A/G snv 4.8E-02 2
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 3
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs10830956 1.000 0.040 11 92947847 intergenic variant C/T snv 0.33 1
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs10838681
NR1H3
1.000 0.040 11 47253513 intron variant G/A snv 0.34 3
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 2
rs10892044
SIK3
1.000 0.040 11 116896183 intron variant T/C snv 0.16 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 1
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 1
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs11066194
HECTD4
1.000 0.040 12 112212323 intron variant A/G snv 4.8E-02 1
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 3
rs11216186
SIK3
1.000 0.040 11 116913976 intron variant T/C snv 7.5E-02 1
rs1127065
CAMK2B
1.000 0.040 7 44220272 synonymous variant C/G;T snv 1.7E-02; 0.41 1
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 1
rs11631342
ALDH1A2 ; LIPC
1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02 1
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 7