Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1208663703
TMPRSS6
0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1161457931
TMPRSS6
0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs11558492
GNPAT
0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs1063303
TRIM5 ; TRIM22
0.925 0.120 11 5698520 missense variant G/A;C;T snv 4.0E-06; 0.50; 1.6E-05 2
rs1060500764
SMAD3
1.000 0.080 15 67181363 missense variant A/G snv 1
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs10336
LOC101928809 ; CXCL9
0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33