Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs17287293
LOC105369698
1.000 0.080 12 24617944 intergenic variant A/G snv 0.12 3
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 2
rs365990
MYH6
1.000 0.080 14 23392602 missense variant A/G snv 0.34 0.45 2
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 2
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 2
rs11154022 6 121427396 intergenic variant A/G;T snv 1
rs11738269 5 179782058 downstream gene variant C/A snv 0.22 1
rs1469020 5 179787023 regulatory region variant G/A snv 0.21 1
rs2745967 1 207955377 upstream gene variant G/A snv 0.60 1
rs7612445 1.000 0.080 3 179455191 upstream gene variant G/T snv 0.24 1
rs6845865
ARHGAP10
4 148053451 intron variant T/C snv 0.27 1
rs6893300
CANX
5 179708814 intron variant C/A snv 0.24 1
rs7735702
CANX
5 179705611 intron variant T/A snv 0.26 1
rs826838
CPNE8
12 38712929 intron variant C/T snv 0.51 1
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 1
rs9320841
LOC105377979
6 121793305 intergenic variant A/G snv 0.23 1
rs9398652
LOC105377979
6 121824888 intergenic variant C/A snv 0.23 1
rs730012
LTC4S
1.000 0.080 5 179793637 upstream gene variant A/C;T snv 1
rs17617068
MAML1
5 179741096 intron variant T/C snv 0.23 1
rs3797776
MAML1
5 179766597 synonymous variant C/T snv 0.24 0.22 1
rs4700838
MAML1
5 179758120 intron variant A/G snv 0.22 1
rs452036
MYH6
14 23396676 intron variant G/A;C snv 0.33 1
rs223116
NGDN
14 23507801 intron variant A/G snv 0.57 1