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: rs56061981
rs56061981
ART3 ; CXCL10
5 0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 0.010 1.000 1 2013 2013
dbSNP: rs6505469
rs6505469
NOS2
1 1.000 0.080 17 27784860 intron variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs6913472
rs6913472 		1 1.000 0.080 6 52232274 downstream gene variant G/A snv 8.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs76980269
rs76980269
NOS1
10 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 0.010 1.000 1 2009 2009
dbSNP: rs7702919
rs7702919
HAVCR1
1 1.000 0.080 5 157059580 upstream gene variant T/C snv 0.56 0.010 1.000 1 2008 2008
dbSNP: rs8019343
rs8019343
RNASE3 ; LOC100507513
2 0.925 0.080 14 20892263 3 prime UTR variant A/T snv 4.2E-02 0.010 1.000 1 2011 2011
dbSNP: rs895819
rs895819
LOC284454 ; MIR23A ; MIR24-2 ; MIR27A
46 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 0.010 1.000 1 2019 2019
dbSNP: rs914142
rs914142
IFNAR1
1 1.000 0.080 21 33353501 intron variant G/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs9429942
rs9429942
CR1
2 0.925 0.080 1 207495285 upstream gene variant C/T snv 0.64 0.010 1.000 1 2008 2008