Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10261922 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 1
rs1110701 1.000 0.120 7 50410929 intergenic variant A/G;T snv 1
rs12887958 1.000 0.120 14 23113360 downstream gene variant C/T snv 0.37 1
rs1569175 1.000 0.120 2 200157231 intergenic variant T/C snv 0.88 1
rs17079534 1.000 0.120 3 39805581 upstream gene variant G/A;C snv 1
rs1945213 1.000 0.120 11 56408195 upstream gene variant C/G;T snv 1
rs4266962 1.000 0.120 10 22052645 intergenic variant C/G;T snv 1
rs4982729 1.000 0.120 14 23107402 upstream gene variant T/C snv 0.66 1
rs4982731 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 1
rs112141546
ADAMTS18
1.000 0.120 16 77367618 missense variant C/A;G;T snv 4.0E-06; 1.4E-03 1
rs4245595
ARID5B
1.000 0.120 10 61963136 intron variant C/T snv 0.69 1
rs7087125
ARID5B
1.000 0.120 10 62013280 intron variant C/T snv 0.37 1
rs7923074
ARID5B
1.000 0.120 10 61963681 intron variant A/C snv 0.56 1
rs141708090
C3orf20
1.000 0.120 3 14761602 missense variant G/T snv 1.9E-03 5.2E-04 1
rs4617118
CCDC26
1.000 0.120 8 129143897 intron variant A/C;G snv 0.20 1
rs73195662
CDHR3
1.000 0.120 7 106018014 missense variant C/A;G;T snv 7.2E-02; 2.0E-05 1
rs2069426
CDKN2B ; CDKN2B-AS1
1.000 0.120 9 22006274 intron variant G/A;C;T snv 4.4E-06; 4.4E-06; 7.5E-02 1
rs2622849
COL11A1
1.000 0.120 1 102955788 intron variant T/A;C;G snv 1
rs10899736
DDC ; FIGNL1
1.000 0.120 7 50479227 intron variant G/A;C snv 1
rs2167364
DDC ; FIGNL1
1.000 0.120 7 50498129 intron variant T/C snv 0.30 1
rs7803247
DDC ; FIGNL1
1.000 0.120 7 50473045 intron variant T/C snv 0.52 1
rs7808025
DDC ; FIGNL1
1.000 0.120 7 50509205 intron variant G/A;C snv 0.28 1
rs45461499
ELOVL1 ; CDC20
1.000 0.120 1 43363065 missense variant G/A;T snv 6.1E-04; 1.6E-03 1
rs11575575
FIGNL1
1.000 0.120 7 50456510 intron variant C/A snv 7.5E-02 1
rs1037351
FIGNL1 ; DDC
1.000 0.120 7 50497706 intron variant T/C snv 0.30 1