Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2285803
rs2285803
0.925 0.160 6 31139481 intron variant T/C snv 0.72
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.810 1.000 2 2013 2014
dbSNP: rs3815087
rs3815087
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.800 1.000 2 2009 2010
dbSNP: rs3815087
rs3815087
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.800 1.000 2 2009 2010
dbSNP: rs3815087
rs3815087
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.800 1.000 2 2009 2010
dbSNP: rs3815087
rs3815087
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.800 1.000 2 2009 2010
dbSNP: rs4959053
rs4959053
0.925 0.280 6 31131800 intron variant G/A snv 6.3E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.800 1.000 2 2012 2013
dbSNP: rs3130573
rs3130573
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
Skin and Connective Tissue Diseases 0.800 1.000 1 2011 2011
dbSNP: rs3815087
rs3815087
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25
CUI: C0038325
Disease: Stevens-Johnson Syndrome
Stevens-Johnson Syndrome
Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders; Stomatognathic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs1265097
rs1265097
6 31138682 missense variant C/A;T snv 0.13; 4.0E-06
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 3 2014 2019
dbSNP: rs149979052
rs149979052
1.000 0.040 6 31137370 intron variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs1966
rs1966
1.000 0.120 6 31139956 3 prime UTR variant C/T snv 0.23 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs3094212
rs3094212
1.000 6 31117993 non coding transcript exon variant G/A snv 0.58
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs3094212
rs3094212
1.000 6 31117993 non coding transcript exon variant G/A snv 0.58
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs3094212
rs3094212
1.000 6 31117993 non coding transcript exon variant G/A snv 0.58
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 2 2009 2010
dbSNP: rs3094212
rs3094212
1.000 6 31117993 non coding transcript exon variant G/A snv 0.58
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
1.000 6 31120157 intron variant G/A;C snv
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
1.000 6 31120157 intron variant G/A;C snv
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
1.000 6 31120157 intron variant G/A;C snv
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
1.000 6 31120157 intron variant G/A;C snv
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs3130559
rs3130559
0.925 0.160 6 31129524 intron variant C/T snv 0.28
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs3130981
rs3130981
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs3130981
rs3130981
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs3130981
rs3130981
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2009 2010
dbSNP: rs3130981
rs3130981
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 2 2009 2010
dbSNP: rs551894425
rs551894425
1.000 6 31117993 non coding transcript exon variant G/A snv
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2009 2010