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: rs1020608562
rs1020608562
CCR5 ; CCR5AS
9 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1369619997
rs1369619997
KIDINS220
1 2 8731746 missense variant G/C snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs2844511
rs2844511 		10 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs374596032
rs374596032
KIDINS220
1 2 8813255 missense variant A/C;G snv 4.0E-06; 8.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs4118325
rs4118325 		1 1 107035210 intergenic variant G/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs527476195
rs527476195
PSORS1C1
6 0.925 0.120 6 31133165 intron variant G/A snv 0.700 1.000 1 2009 2009
dbSNP: rs6467710
rs6467710
DGKI
1 7 137519073 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs763059810
rs763059810
CXCR4
41 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs767830104
rs767830104
CXCR4
13 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs909253
rs909253
LTA ; LOC100287329
34 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs919266
rs919266
BST2
1 19 17403506 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs9261290
rs9261290
RNF39
10 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 0.700 1.000 1 2009 2009
dbSNP: rs2395029
rs2395029
HCP5
12 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 0.800 1.000 1 2009 2009
dbSNP: rs9368699
rs9368699
SNORD48 ; SNHG32
8 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs13194504
rs13194504 		3 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs3117143
rs3117143
LOC100129636
4 0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs3749971
rs3749971
OR5V1 ; OR12D3
4 0.925 0.160 6 29374998 missense variant G/A snv 5.5E-02 5.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs8321
rs8321
ZNRD1
16 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 0.800 1.000 1 2009 2009
dbSNP: rs1235162
rs1235162
GABBR1
6 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs3130380
rs3130380
HCG18 ; HCG17
10 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs3093662
rs3093662
TNF
9 0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs3131093
rs3131093 		3 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs4324798
rs4324798 		8 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs1233579
rs1233579 		3 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2009 2009