Source: GWASDB

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: rs2854275
rs2854275
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.800 1.000 1 2013 2013
dbSNP: rs9274407
rs9274407
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77
Chemical and Drug Induced Liver Injury
0.800 1.000 1 2011 2011
dbSNP: rs1063355
rs1063355
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2009
dbSNP: rs1063355
rs1063355
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2013 2013
dbSNP: rs201386475
rs201386475
1.000 0.120 6 32668286 5 prime UTR variant -/CA delins
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs2515895
rs2515895
1.000 0.040 6 32661183 intron variant T/C snv 0.24
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs2854272
rs2854272
1.000 0.040 6 32661903 non coding transcript exon variant A/G snv 0.38
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs3189152
rs3189152
1.000 0.080 6 32666564 missense variant A/G;T snv 0.19 0.39
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.700 1.000 1 2013 2013
dbSNP: rs3828800
rs3828800
1.000 0.120 6 32668286 5 prime UTR variant G/A snv 0.20
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3891175
rs3891175
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs3891175
rs3891175
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2013 2013
dbSNP: rs4988888
rs4988888
1.000 0.040 6 32667420 intron variant T/C snv 0.20
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs9274407
rs9274407
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 1.000 1 2013 2013
dbSNP: rs9274614
rs9274614
1.000 0.120 6 32668069 intron variant C/A;G snv
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
0.700 1.000 1 2012 2012
dbSNP: rs9282114
rs9282114
1.000 0.040 6 32661903 non coding transcript exon variant -/C ins
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012