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: rs1048412
rs1048412
ZNRD1
1 1.000 6 30064718 3 prime UTR variant A/G snv 0.15 0.17 0.010 1.000 1 2010 2010
dbSNP: rs10892151
rs10892151
DSCAML1 ; LOC105369515
3 1.000 11 117661016 intron variant C/T snv 9.7E-02 0.010 < 0.001 1 2011 2011
dbSNP: rs1272938495
rs1272938495
CXCR4 ; LOC112268426
1 1.000 2 136115225 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1276738522
rs1276738522
CD9 ; LOC105369625
1 1.000 12 6232664 start lost A/G snv 4.9E-06 0.010 1.000 1 2001 2001
dbSNP: rs1292288729
rs1292288729
CYP2B6
1 1.000 19 41009375 missense variant T/C snv 7.4E-06 0.010 1.000 1 2011 2011
dbSNP: rs1433591886
rs1433591886
PPIG
1 1.000 2 169633213 missense variant G/A snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs3740996
rs3740996
TRIM5
1 1.000 11 5680051 missense variant G/A snv 0.13 0.10 0.010 1.000 1 2007 2007
dbSNP: rs4657412
rs4657412
LMX1A ; LMX1A-AS2
1 1.000 1 165207796 intron variant G/A snv 0.79 0.010 1.000 1 2017 2017
dbSNP: rs57302492
rs57302492
CD207
1 1.000 2 70831099 missense variant T/A snv 7.0E-02 8.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs749569169
rs749569169
CHN2 ; LOC107986700
1 1.000 7 29512676 missense variant A/G snv 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs756151230
rs756151230
ERVW-1 ; GATAD1
1 1.000 7 92470377 missense variant G/C snv 0.010 1.000 1 2001 2001
dbSNP: rs774027752
rs774027752
CYP2A6
1 1.000 19 40845472 missense variant T/C snv 8.0E-06 1.4E-05 0.010 1.000 1 2012 2012
dbSNP: rs1188975135
rs1188975135
APOBEC3C ; APOBEC3F
4 0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1194919682
rs1194919682
CXCR4 ; LOC112268426
2 0.925 0.040 2 136115158 missense variant A/G snv 0.010 1.000 1 2011 2011
dbSNP: rs11881222
rs11881222
IFNL3
3 0.925 0.080 19 39244283 intron variant A/G snv 0.30 0.010 1.000 1 2013 2013
dbSNP: rs1799972
rs1799972
OPRM1
6 0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs7248668
rs7248668 		3 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 0.010 1.000 1 2013 2013
dbSNP: rs11045819
rs11045819
SLCO1B1
4 0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs4619915
rs4619915
ART3 ; CXCL11
3 0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 0.010 1.000 1 2015 2015
dbSNP: rs10833
rs10833
IL15
10 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs14158
rs14158
LDLR
5 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 0.010 1.000 1 2013 2013
dbSNP: rs1126477
rs1126477
LTF
7 0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 0.010 1.000 1 2015 2015
dbSNP: rs10336
rs10336
CXCL9 ; LOC101928809
4 0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1126478
rs1126478
LTF
11 0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 0.010 1.000 1 2015 2015
dbSNP: rs12252
rs12252
IFITM3
23 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 0.010 1.000 1 2018 2018