Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs10056340 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 3
rs1042718
ADRB2
0.925 0.080 5 148827354 missense variant C/A;T snv 0.23; 4.0E-06 3
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 3
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 3
rs1158867
PROC
1.000 0.080 2 127419801 splice region variant C/T snv 0.51 3
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18 3
rs12952581
LOC102724596
0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv 3
rs1538660
ELP1
0.882 0.080 9 108879545 missense variant G/A snv 0.19 0.22 3
rs1612986 0.925 0.080 10 9022753 intergenic variant T/C snv 0.24 3
rs1655558
ITPKA
0.925 0.080 15 41495387 intron variant T/G snv 0.66 3
rs17154353
SLC26A4
0.925 0.080 7 107710182 missense variant G/A;T snv 3.7E-03; 8.0E-06 3
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs200039720
SFTPC
0.925 0.080 8 22162688 missense variant G/A snv 1.5E-04 1.0E-04 3
rs2233407
NFKBIA
0.882 0.080 14 35405317 upstream gene variant T/A;C snv 3
rs2280091
ADAM33
0.882 0.080 20 3669587 missense variant A/G snv 0.13 0.14 3
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs347412
DGKH
1.000 0.080 13 42212544 intron variant A/G;T snv 3
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs3771175
IL1RL1 ; IL18R1
0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 3
rs3856439
LINC00299
0.925 0.080 2 8319274 intron variant C/A;T snv 0.29 3