Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs12504244 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 2
rs5030980 0.925 0.120 16 67483042 missense variant C/T snv 3.2E-02 2.9E-02 2
rs75063949 0.925 0.040 6 25590813 intron variant C/G snv 0.14 2
rs4633 0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 2
rs929626 0.925 0.120 5 158883623 intron variant A/G snv 0.40 2
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 2
rs11174202 0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs10747478 1.000 0.040 1 96435899 intergenic variant T/A;C;G snv 1
rs1285957 1.000 0.040 7 141889478 downstream gene variant T/C snv 0.86 1
rs13100344 1.000 0.040 3 94886263 intergenic variant T/A snv 0.40 1
rs145241704 1.000 0.040 7 141805287 upstream gene variant T/G snv 7.4E-02 1
rs370838138 1.000 0.040 5 25081736 intergenic variant G/C snv 0.42 1
rs4622308 0.925 0.160 12 56075401 upstream gene variant C/T snv 1
rs56156506 1.000 0.040 X 38140399 intron variant A/T snv 0.33 1
rs62090893 1.000 0.040 18 75338379 intergenic variant G/A snv 9.7E-02 1
rs6589488 1.000 0.040 11 115226236 intron variant A/T snv 0.90 1
rs2287348 1.000 0.040 2 53812676 intron variant C/A;T snv 1
rs9874207 1.000 0.040 3 70970599 non coding transcript exon variant T/C snv 0.64 1
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 1
rs117957029 1.000 0.040 12 127200688 intron variant T/C snv 1.4E-02 1
rs200312312 1.000 0.040 5 104666645 intron variant T/C snv 0.16 1
rs2008387 1.000 0.040 10 129650500 intron variant G/A snv 0.36 1
rs9821797 1.000 0.040 3 48680820 intron variant T/A snv 0.20 1