Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 2
rs10246797
SUGCT
7 40304762 intron variant C/A;G snv 0.45 1
rs10248619
GRB10
7 50683393 intron variant T/C snv 0.71 1
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs10500292
SYMPK
19 45824675 intron variant C/T snv 0.46 2
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 1
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11039119
MIR6745 ; PACSIN3
11 47180373 intron variant G/A snv 0.38 0.33 2
rs11039130 11 47207765 intergenic variant C/T snv 0.20 2
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 1
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs1120557 14 62662722 regulatory region variant A/G snv 0.88 1
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs11571943
CDC5L
6 44403953 synonymous variant T/C snv 2.1E-02 2.9E-02 1
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3