Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12219080
rs12219080
SFTPD
1 1.000 0.040 10 79949523 intron variant C/T snv 8.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs17886286
rs17886286
SFTPD
1 1.000 0.040 10 79944096 intron variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs2233406
rs2233406
NFKBIA
12 0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26 0.010 1.000 1 2007 2007
dbSNP: rs3138053
rs3138053
NFKBIA
10 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 0.010 1.000 1 2007 2007
dbSNP: rs4251961
rs4251961
IL1RN
10 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2011 2011
dbSNP: rs4925858
rs4925858 		1 1.000 0.040 8 144446548 upstream gene variant G/A snv 0.44 0.010 1.000 1 2010 2010
dbSNP: rs600718
rs600718
NFKBIZ
1 1.000 0.040 3 101851531 intron variant A/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs616597
rs616597
NFKBIZ
1 1.000 0.040 3 101850882 intron variant A/C snv 0.82 0.010 1.000 1 2010 2010
dbSNP: rs760477
rs760477
TONSL
1 1.000 0.040 8 144443060 intron variant G/A snv 0.41 0.010 1.000 1 2010 2010