Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10178332
ROCK2
0.925 0.120 2 11268891 intron variant C/A;G snv 2
rs17135889
ABCA3
0.925 0.080 16 2337259 intron variant G/A snv 0.11 2
rs170447
ABCA3
1.000 0.080 16 2299370 intron variant T/C snv 0.51 0.45 1
rs1923537 1.000 0.080 10 79935452 intron variant A/G snv 0.37 1
rs313909
ABCA3
1.000 0.080 16 2287992 intron variant G/A;C snv 0.42; 4.3E-06 1
rs726843
ROCK2
1.000 0.080 2 11216064 intron variant G/A snv 0.38 1
rs7956915
SCNN1A
1.000 0.080 12 6361094 intron variant A/G snv 0.52 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs121917834
SFTPC
0.790 0.080 8 22163096 missense variant T/A;C snv 3.6E-05 10
rs149989682
ABCA3
0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 10
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs1130866
SFTPB
0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs1966265
FGFR4
0.827 0.160 5 177089630 missense variant G/A;T snv 0.25 8
rs121918563
PRPH2
0.827 0.120 6 42721781 missense variant A/G snv 8.0E-06 1.4E-05 6
rs533117495
ABCB1
0.827 0.200 7 87595783 missense variant C/T snv 8.0E-06 5
rs117603931
ABCA3
0.882 0.080 16 2319591 missense variant C/T snv 5.7E-03 6.5E-03 4
rs1322403577
SFTPA1
0.882 0.120 10 79613818 missense variant T/C snv 4.0E-06 4
rs1124
SFTPC ; BMP1
0.882 0.160 8 22164004 missense variant G/A snv 0.30 0.26 3
rs146709251
ABCA3
0.882 0.080 16 2279070 missense variant G/A snv 4.3E-03 3.0E-03 3
rs761495176
NR3C1
0.882 0.080 5 143400263 missense variant T/C snv 1.7E-05 3
rs1042689672
SFTPA2
0.925 0.080 10 79557504 missense variant A/G snv 7.0E-06 2
rs35768389
ROCK2
0.925 0.160 2 11214974 missense variant T/A snv 3.5E-04 3.6E-04 2
rs2271255
ROCK1
1.000 0.080 18 21044113 missense variant T/C snv 3.6E-05 7.0E-06 1