Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10788165 0.925 0.080 10 121284700 regulatory region variant T/G snv 0.35 2
rs118004742
EFCAB13
0.925 0.080 17 47391492 stop gained T/G snv 4.4E-02 4.2E-02 2
rs1184094026
RASSF1
0.925 0.080 3 50331675 missense variant T/G snv 8.0E-06 1.4E-05 2
rs13112099
UGT2B15
0.925 0.080 4 68672015 upstream gene variant T/G snv 0.53 2
rs2387084 0.925 0.080 16 74054192 non coding transcript exon variant T/G snv 0.28 2
rs4473733
GUSBP1
0.925 0.080 5 21567711 intron variant T/G snv 2
rs62113214
KLK3
0.925 0.080 19 50859281 intron variant T/G snv 4.9E-02 2
rs7837688 0.925 0.080 8 127527115 intergenic variant T/G snv 0.91 2
rs79670217
ZNF652
0.925 0.080 17 49337732 intron variant T/G snv 3.7E-02 2
rs9296068 0.925 0.200 6 33020918 intergenic variant T/G snv 0.42 2
rs11691517
MIR4435-2HG ; BCL2L11
1.000 0.080 2 111135519 intron variant T/G snv 0.22 1
rs11859370
ADGRG1
1.000 0.080 16 57619621 intron variant T/G snv 8.4E-02 1
rs12682344
PCAT1 ; CASC19
1.000 0.080 8 127094539 intron variant T/G snv 0.13 1
rs71277158
PRKCI
1.000 0.080 3 170281428 non coding transcript exon variant T/G snv 0.12 1
rs723557 1.000 0.080 X 127519376 intergenic variant T/G snv 7.2E-02 1
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs3803185
ARL11
0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41 5
rs55829688
SNORD77 ; SNORA103 ; ZBTB37 ; SNORD76 ; SNORD74 ; SNORD75 ; GAS5
0.827 0.200 1 173868168 5 prime UTR variant T/C;G snv 5
rs1060501201
TP53
0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs4705342
MIR143 ; CARMN
0.851 0.160 5 149428408 non coding transcript exon variant T/C;G snv 4