Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs35859536
LOC105375716
8 117179236 downstream gene variant C/T snv 0.25 2
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 1
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs12385797 11 106465562 upstream gene variant C/A snv 6.4E-02 1
rs234148
LOC105370650
14 97688682 upstream gene variant T/C;G snv 1
rs6048205
LINC00261
1.000 0.080 20 22578963 upstream gene variant A/G snv 9.1E-02 1
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
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs2292910
CRY2
1.000 0.080 11 45882062 3 prime UTR variant A/C snv 0.66 2
rs3778321
RREB1
6 7250037 3 prime UTR variant G/A snv 0.11 2
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs2280231
KBTBD4 ; NDUFS3
11 47578886 5 prime UTR variant C/T snv 0.24 0.20 2
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 1
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs11571943
CDC5L
6 44403953 synonymous variant T/C snv 2.1E-02 2.9E-02 1
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs17762454
RREB1
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4