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: rs353163
rs353163
TMPRSS11A ; UBA6-AS1
4 0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 0.020 1.000 2 2006 2013
dbSNP: rs1014867
rs1014867
FAT4
3 0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 0.010 1.000 1 2013 2013
dbSNP: rs1039808
rs1039808
FAT4
3 0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 0.010 1.000 1 2013 2013
dbSNP: rs10437048
rs10437048
PADI4
1 1.000 0.080 1 17356224 intron variant A/C snv 0.010 1.000 1 2011 2011
dbSNP: rs10509670
rs10509670
PLCE1
5 0.851 0.080 10 94308190 intron variant A/G snv 0.30 0.010 1.000 1 2019 2019
dbSNP: rs10953615
rs10953615 		1 1.000 0.080 7 109512654 intergenic variant A/G snv 0.29 0.010 1.000 1 2016 2016
dbSNP: rs11473
rs11473
BSG
4 0.882 0.080 19 582982 3 prime UTR variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs11548103
rs11548103
S100A14
4 0.882 0.080 1 153615864 splice region variant C/T snv 0.40 0.39 0.010 1.000 1 2017 2017
dbSNP: rs121918714
rs121918714
TGFBR2
1 1.000 0.080 3 30691471 missense variant G/C snv 0.710 1.000 1 2000 2000
dbSNP: rs12508222
rs12508222
FAT4
3 0.925 0.080 4 125449492 missense variant G/A;T snv 4.3E-02; 2.0E-05 0.010 1.000 1 2013 2013
dbSNP: rs13016963
rs13016963
FLACC1
5 0.851 0.080 2 201298088 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017
dbSNP: rs13294589
rs13294589 		1 1.000 0.080 9 26694890 intergenic variant A/G snv 0.20 0.010 1.000 1 2016 2016
dbSNP: rs1567047
rs1567047
FAT4
3 0.925 0.080 4 125451587 missense variant G/A snv 0.27 0.22 0.010 1.000 1 2013 2013
dbSNP: rs1595066
rs1595066
ERBB4
4 0.882 0.080 2 211377000 3 prime UTR variant C/T snv 0.28 0.010 1.000 1 2014 2014
dbSNP: rs16845990
rs16845990
ERBB4
4 0.882 0.080 2 211378286 3 prime UTR variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs2228059
rs2228059
IL15RA ; LOC107984200
5 0.882 0.080 10 5960405 missense variant T/G snv 0.51 0.55 0.010 1.000 1 2014 2014
dbSNP: rs2244438
rs2244438
TRAK2
4 0.882 0.080 2 201387816 missense variant G/A;T snv 0.29; 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs2274224
rs2274224
PLCE1 ; PLCE1-AS1
6 0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 0.010 1.000 1 2013 2013
dbSNP: rs2320615
rs2320615
NAF1
3 0.925 0.080 4 163148797 intron variant A/G snv 0.78 0.010 1.000 1 2017 2017
dbSNP: rs2477134
rs2477134
PADI4
1 1.000 0.080 1 17307077 upstream gene variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs2501796
rs2501796
PADI4
1 1.000 0.080 1 17307027 upstream gene variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs312986
rs312986 		3 0.925 0.080 18 1898710 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs31564
rs31564
IL9
3 0.925 0.080 5 135894564 intron variant G/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs3738894
rs3738894
PRKCE
4 0.882 0.080 2 46187030 3 prime UTR variant G/A snv 1.1E-02 0.010 1.000 1 2020 2020
dbSNP: rs41265997
rs41265997
PADI4
1 1.000 0.080 1 17342111 missense variant C/G;T snv 4.0E-06; 1.6E-05 0.010 1.000 1 2011 2011