Disease: Bronchopulmonary Dysplasia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs7224199
SLC6A4
0.827 0.160 17 30196708 3 prime UTR variant G/T snv 0.49 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs4500567
TSPAN8
0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs1705236
TSPAN8
0.827 0.200 12 71151778 intron variant T/A snv 7.6E-02 5
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4
rs12290811
TENM4
0.882 0.120 11 79372576 intron variant T/A snv 0.18 3
rs78089757 0.882 0.120 10 125424260 intergenic variant G/A snv 9.9E-03 3