Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12
rs2488457
AP4B1-AS1 ; PTPN22
0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs3789604
RSBN1 ; AP4B1-AS1
0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs222747
TRPV1
0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs11154178
LOC105377982 ; TRDN
0.807 0.240 6 123540174 intron variant T/A;C snv 7
rs13306190
APOB
0.807 0.320 2 21032408 missense variant G/A;C;T snv 1.7E-04; 8.0E-06 7
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs80028505
MAPK14
0.807 0.240 6 36030611 intron variant C/G;T snv 7
rs121909800
VDR
0.807 0.360 12 47844859 missense variant G/A;T snv 6