Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs3130968 1.000 0.040 6 31097294 regulatory region variant C/G;T snv 2
rs4842266 12 79557786 upstream gene variant G/A snv 0.50 2
rs6668352 1 11854772 downstream gene variant G/A snv 0.24 2
rs10467515 13 52927172 regulatory region variant A/G snv 1.2E-02 1
rs138294113 19 11081053 downstream gene variant C/T snv 0.12 1
rs1638665 10 117414434 regulatory region variant T/C snv 2.9E-02 1
rs16837982 2 154682843 intergenic variant G/T snv 5.5E-02 1
rs16890431 4 14429763 intron variant A/G snv 4.5E-02 1
rs4722172 7 22746913 downstream gene variant G/A snv 0.87 1
rs55784307 14 70034647 downstream gene variant C/A snv 0.16 1
rs62084752 17 68093252 upstream gene variant C/A;G snv 1
rs634138 2 160876023 upstream gene variant C/T snv 2.2E-02 1
rs736088 6 25896941 intergenic variant T/C snv 1.0E-02 1
rs7787478 7 97601785 upstream gene variant T/C snv 0.13 1
rs9356334 6 165000406 intron variant T/G snv 2.6E-02 1
rs9567406 13 44303182 intergenic variant A/G;T snv 0.15 1
rs9596720 13 52924312 regulatory region variant C/T snv 1.5E-02 1
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 7
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41