Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117603931
ABCA3
0.882 0.080 16 2319591 missense variant C/T snv 5.7E-03 6.5E-03 4
rs28451617
ZSCAN25 ; CYP3A7-CYP3A51P ; CYP3A7
0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02 4
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
rs13332514
ABCA3
0.925 0.080 16 2317335 synonymous variant G/A snv 0.17 0.12 2
rs1966265
FGFR4
0.827 0.160 5 177089630 missense variant G/A;T snv 0.25 8
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs1124
SFTPC ; BMP1
0.882 0.160 8 22164004 missense variant G/A snv 0.30 0.26 3
rs1130866
SFTPB
0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs170447
ABCA3
1.000 0.080 16 2299370 intron variant T/C snv 0.51 0.45 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246