Source: ALL

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: rs12191877
rs12191877
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.830 1.000 5 2009 2015
dbSNP: rs2524079
rs2524079
6 31274397 intron variant G/A snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.800 1.000 4 2011 2019
dbSNP: rs2428494
rs2428494
0.827 0.160 6 31354420 intron variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 3 2016 2019
dbSNP: rs9468925
rs9468925
0.851 0.040 6 31291060 intron variant G/A snv 0.44
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.820 1.000 3 2010 2012
dbSNP: rs12191877
rs12191877
0.851 0.120 6 31285148 intron variant C/T snv 0.12
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
0.851 0.120 6 31285148 intron variant C/T snv 0.12
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
0.851 0.120 6 31285148 intron variant C/T snv 0.12
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 2 2009 2010
dbSNP: rs2156875
rs2156875
0.882 0.200 6 31349570 intron variant C/T snv 0.50
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2009
dbSNP: rs2523619
rs2523619
0.925 0.120 6 31350367 intron variant T/C snv 0.23
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2009
dbSNP: rs2524079
rs2524079
6 31274397 intron variant G/A snv 0.44
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 2 2011 2017
dbSNP: rs2853946
rs2853946
6 31279426 intron variant A/G;T snv 0.37
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 2 2014 2019
dbSNP: rs3134792
rs3134792
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.800 1.000 2 2007 2008
dbSNP: rs3819299
rs3819299
1.000 6 31354590 non coding transcript exon variant T/G snv 7.7E-02 2.3E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 2 2011 2016
dbSNP: rs7382297
rs7382297
0.925 0.080 6 31279290 intron variant T/C;G snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 2 2007 2010
dbSNP: rs9468925
rs9468925
0.851 0.040 6 31291060 intron variant G/A snv 0.44
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
0.020 1.000 2 2011 2012
dbSNP: rs1055821
rs1055821
1.000 0.040 6 31354142 3 prime UTR variant G/T snv 5.6E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.010 1.000 1 2017 2017
dbSNP: rs1058026
rs1058026
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 1 2010 2010
dbSNP: rs1058026
rs1058026
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs1058026
rs1058026
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 1 2010 2010
dbSNP: rs1058026
rs1058026
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 1 2010 2010
dbSNP: rs1058026
rs1058026
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 1 2010 2010
dbSNP: rs1093
rs1093
1.000 0.080 6 31354129 3 prime UTR variant A/G snv 0.15
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs111721712
rs111721712
6 31347630 intron variant -/T delins 0.55
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs114398276
rs114398276
6 31279046 intron variant A/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2018 2018