Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs11211480
TAL1
1 47227548 non coding transcript exon variant A/G snv 0.42 4
rs2492301
LINC01137 ; ZC3H12A
1 37473572 intron variant T/C snv 0.53 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 3
rs72755295
EXO1
1.000 0.080 1 241870961 intron variant A/G snv 2.1E-02 3
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs10923397 1 117708521 regulatory region variant C/T snv 0.14 2
rs11811522
SPTA1
1 158634353 intron variant G/A snv 0.35 2
rs12127588 1 198626376 intergenic variant G/A;C;T snv 2
rs12563213 1 154318779 upstream gene variant G/C snv 0.30 2
rs140446749
SPTA1
1 158668470 intron variant G/A snv 8.0E-03 2
rs1578741 1 117716081 intergenic variant A/C snv 0.19 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs2502994
CNR2
1 23872873 3 prime UTR variant T/A;C snv 2
rs34544423 1 198578103 regulatory region variant C/G snv 6.4E-02 2
rs35229050
E2F2
1 23514124 intron variant AA/-;A;AAA delins 0.53 2
rs35340377
TRIM58
1 247874908 intron variant G/A snv 0.23 2
rs3916164 1 39604267 intergenic variant G/A snv 0.24 2
rs3962382 1 67700010 downstream gene variant A/C;G snv 2
rs646179
USP1
1 62437203 5 prime UTR variant A/G;T snv 2