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: rs9263739
rs9263739
CCHCR1
1.000 0.040 6 31143579 intron variant C/T snv 0.16
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 1 2009 2009
dbSNP: rs1265110
rs1265110
CCHCR1
1.000 0.120 6 31151645 intron variant C/T snv 0.14
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2009
dbSNP: rs130067
rs130067
CCHCR1
0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 2 2007 2009
dbSNP: rs720465
rs720465
TCF19 ; CCHCR1
1.000 6 31158000 splice region variant C/A snv 0.29
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 2 2009 2010
dbSNP: rs720465
rs720465
TCF19 ; CCHCR1
1.000 6 31158000 splice region variant C/A snv 0.29
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs720465
rs720465
TCF19 ; CCHCR1
1.000 6 31158000 splice region variant C/A snv 0.29
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs720465
rs720465
TCF19 ; CCHCR1
1.000 6 31158000 splice region variant C/A snv 0.29
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 2 2009 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.700 1.000 1 2013 2013
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs1265115
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs130065
rs130065
CCHCR1
0.925 0.120 6 31154723 missense variant G/A snv 0.15 0.16
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010
dbSNP: rs130065
rs130065
CCHCR1
0.925 0.120 6 31154723 missense variant G/A snv 0.15 0.16
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2010 2010
dbSNP: rs130067
rs130067
CCHCR1
0.851 0.200 6 31150734 missense variant T/G snv 0.23 0.21
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 1 2011 2011
dbSNP: rs130072
rs130072
CCHCR1
1.000 6 31144707 missense variant C/T snv 0.10 8.4E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs130072
rs130072
CCHCR1
1.000 6 31144707 missense variant C/T snv 0.10 8.4E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs130072
rs130072
CCHCR1
1.000 6 31144707 missense variant C/T snv 0.10 8.4E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs130072
rs130072
CCHCR1
1.000 6 31144707 missense variant C/T snv 0.10 8.4E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs130078
rs130078
CCHCR1
1.000 0.120 6 31150788 synonymous variant C/G snv 0.74 0.75
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2073716
rs2073716
CCHCR1
1.000 0.200 6 31155220 intron variant C/G snv 6.8E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2012 2012
dbSNP: rs2240064
rs2240064
CCHCR1
1.000 0.120 6 31146796 intron variant G/A;T snv
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2013 2013
dbSNP: rs3094187
rs3094187
TCF19 ; CCHCR1
0.925 0.120 6 31159167 5 prime UTR variant C/T snv 0.55
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs3094187
rs3094187
TCF19 ; CCHCR1
0.925 0.120 6 31159167 5 prime UTR variant C/T snv 0.55
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2009 2009
dbSNP: rs3094187
rs3094187
TCF19 ; CCHCR1
0.925 0.120 6 31159167 5 prime UTR variant C/T snv 0.55
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2011 2011