Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs73110464
KRT8
0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs2974935
MTX1
0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 16
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 14
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs121913224
APC
0.742 0.200 5 112839515 frameshift variant AAAGA/- delins 13
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 13
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38 12
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12