Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs29232
rs29232
0.925 0.240 6 29643654 intergenic variant C/T snv 0.39
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.740 1.000 2 2009 2018
dbSNP: rs6774494
rs6774494
0.882 0.160 3 169364845 intron variant G/A snv 0.42
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.740 1.000 1 2010 2017
dbSNP: rs9510787
rs9510787
1.000 0.120 13 23631056 intron variant A/G snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.730 1.000 1 2010 2018
dbSNP: rs3869062
rs3869062
1.000 0.120 6 29967114 downstream gene variant A/G snv 5.5E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 3 2009 2017
dbSNP: rs3129055
rs3129055
1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 2 2009 2017
dbSNP: rs1412829
rs1412829
0.742 0.400 9 22043927 intron variant A/G snv 0.28
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 1 2010 2017
dbSNP: rs2860580
rs2860580
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 1 2010 2017
dbSNP: rs2894207
rs2894207
0.882 0.160 6 31295974 intron variant T/C snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 1 2010 2018
dbSNP: rs31489
rs31489
0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 1 2010 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 1 2010 2016
dbSNP: rs2517713
rs2517713
1.000 0.120 6 29950322 downstream gene variant G/A;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 3 2009 2015
dbSNP: rs189897
rs189897
1.000 0.120 3 37477054 intron variant T/A snv 0.13
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 2 2009 2010
dbSNP: rs16896923
rs16896923
1.000 0.120 6 30032910 non coding transcript exon variant T/C snv 5.0E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 1 2010 2017
dbSNP: rs2076483
rs2076483
0.925 0.240 6 29603768 intron variant A/C;G snv 3.1E-05; 0.13
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 1 2010 2017
dbSNP: rs2212020
rs2212020
1.000 0.120 3 37475971 intron variant C/T snv 0.34
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 1 2009 2009
dbSNP: rs28421666
rs28421666
1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 1 2010 2017
dbSNP: rs4977756
rs4977756
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.710 1.000 1 2010 2016
dbSNP: rs5009448
rs5009448
1.000 0.120 6 29972711 upstream gene variant T/C snv 0.74
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 3 2009 2012
dbSNP: rs9260734
rs9260734
1.000 0.120 6 29964889 intergenic variant G/A snv 0.22
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 3 2009 2012
dbSNP: rs29230
rs29230
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 2 2010 2012
dbSNP: rs3131866
rs3131866
1.000 0.120 6 29703963 downstream gene variant G/A snv 0.24
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 2 2009 2010
dbSNP: rs417162
rs417162
1.000 0.120 6 29948728 downstream gene variant C/T snv 0.66
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 2 2009 2012
dbSNP: rs10163267
rs10163267
1.000 0.120 16 83940313 intron variant G/A;C snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs1016343
rs1016343
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010