Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs2292910
CRY2
1.000 0.080 11 45882062 3 prime UTR variant A/C snv 0.66 2
rs3736594
MRPL33
2 27772914 intron variant A/C snv 0.62 2
rs9981885 21 18958319 intron variant A/C snv 0.22 1
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs7867224
GLIS3
9 4292152 intron variant A/C;G snv 0.37 2
rs2018860
IGF1R
0.925 0.120 15 98715481 intron variant A/C;G;T snv 2
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 3
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 3
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs2605627
SMCO4
11 93526349 intron variant A/G snv 0.79 2
rs7101470
C11orf49
11 47032897 intron variant A/G snv 7.4E-02 2
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 2
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 1
rs1120557 14 62662722 regulatory region variant A/G snv 0.88 1
rs17066694 5 166334297 intergenic variant A/G snv 4.8E-02 1