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: rs10754558
rs10754558
NLRP3
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs11206510
rs11206510 		16 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 0.010 1.000 1 2010 2010
dbSNP: rs11265260
rs11265260 		2 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 0.010 1.000 1 2018 2018
dbSNP: rs1130864
rs1130864
CRP
27 0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 0.010 1.000 1 2014 2014
dbSNP: rs1137100
rs1137100
LEPR
39 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2015 2015
dbSNP: rs1137101
rs1137101
LEPR
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2015 2015
dbSNP: rs11583680
rs11583680
PCSK9
3 0.882 0.200 1 55039995 missense variant C/G;T snv 1.6E-05; 0.11 0.010 1.000 1 2019 2019
dbSNP: rs11591147
rs11591147
PCSK9
28 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 0.010 1.000 1 2018 2018
dbSNP: rs12083537
rs12083537
IL6R
4 0.882 0.200 1 154408627 intron variant A/G snv 0.22 0.010 1.000 1 2020 2020
dbSNP: rs12122341
rs12122341 		2 1.000 0.080 1 115113069 regulatory region variant C/G snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs12128240
rs12128240
MIR34A ; MIR34AHG
1 1.000 0.080 1 9151244 non coding transcript exon variant C/G;T snv 0.010 < 0.001 1 2019 2019
dbSNP: rs12130333
rs12130333 		4 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 0.010 1.000 1 2011 2011
dbSNP: rs12904
rs12904
EFNA1 ; SLC50A1
5 0.827 0.160 1 155134221 3 prime UTR variant G/A snv 0.40 0.010 1.000 1 2019 2019
dbSNP: rs1324214
rs1324214
F3
3 0.925 0.120 1 94531732 intron variant G/A snv 0.21 0.010 1.000 1 2009 2009
dbSNP: rs1341665
rs1341665 		2 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 0.010 1.000 1 2006 2006
dbSNP: rs138364069
rs138364069
FAF1
1 1.000 0.080 1 50832533 intron variant C/T snv 1.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs1396616608
rs1396616608
YY1AP1
1 1.000 0.080 1 155660237 frameshift variant G/- delins 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs142884651
rs142884651
MTHFR ; C1orf167
1 1.000 0.080 1 11786327 3 prime UTR variant G/A snv 0.010 1.000 1 2018 2018
dbSNP: rs143101792
rs143101792
CRP
5 0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 0.010 1.000 1 2015 2015
dbSNP: rs145204276
rs145204276
GAS5 ; ZBTB37 ; SNORD74 ; SNORD75 ; SNORD76 ; SNORD77 ; SNORA103
31 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 0.010 1.000 1 2018 2018
dbSNP: rs147270785
rs147270785
MASP2
2 1.000 0.080 1 11046616 missense variant G/A snv 6.5E-04 6.4E-04 0.010 1.000 1 2018 2018
dbSNP: rs1554286
rs1554286
IL10 ; IL19
7 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 0.010 1.000 1 2013 2013
dbSNP: rs161810
rs161810
TNFRSF9
4 0.925 0.120 1 7940737 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs161818
rs161818
TNFRSF9
1 1.000 0.080 1 7927492 intron variant T/C snv 9.7E-02 0.010 1.000 1 2017 2017
dbSNP: rs17114036
rs17114036
PLPP3
5 0.851 0.120 1 56497149 intron variant A/G snv 0.11 0.010 1.000 1 2018 2018