Source: GWASCAT

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: rs114012716
rs114012716
HCP5
1.000 0.080 6 31466589 non coding transcript exon variant G/A snv
CUI: C0027121
Disease: Myositis
Myositis 		0.700 1.000 1 2015 2015
dbSNP: rs114277634
rs114277634
HCP5
1.000 0.040 6 31474954 intron variant T/A;C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs114277634
rs114277634
HCP5
1.000 0.040 6 31474954 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs114864815
rs114864815
HCP5
6 31461210 intron variant C/T snv
CUI: C0019360
Disease: Herpes zoster disease
Herpes zoster disease 		0.700 1.000 1 2015 2015
dbSNP: rs115146037
rs115146037
HCP5
1.000 0.080 6 31466554 non coding transcript exon variant A/T snv
CUI: C0027121
Disease: Myositis
Myositis 		0.700 1.000 1 2015 2015
dbSNP: rs115902351
rs115902351
HCP5
1.000 0.080 6 31466844 non coding transcript exon variant A/G snv
CUI: C0027121
Disease: Myositis
Myositis 		0.700 1.000 1 2015 2015
dbSNP: rs116088953
rs116088953
HCP5
1.000 0.080 6 31475005 intron variant G/A snv
CUI: C0027121
Disease: Myositis
Myositis 		0.700 1.000 1 2015 2015
dbSNP: rs116822326
rs116822326
HCP5
0.925 0.080 6 31466334 non coding transcript exon variant A/G snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs116822326
rs116822326
HCP5
0.925 0.080 6 31466334 non coding transcript exon variant A/G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2017 2017
dbSNP: rs2523673
rs2523673
HCP5
6 31469218 non coding transcript exon variant T/C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2596449
rs2596449
HCP5 ; HCG26
0.925 0.160 6 31470613 non coding transcript exon variant A/G snv 0.79
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2015 2015
dbSNP: rs2596449
rs2596449
HCP5 ; HCG26
0.925 0.160 6 31470613 non coding transcript exon variant A/G snv 0.79
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia 		0.700 1.000 1 2015 2015
dbSNP: rs3094013
rs3094013
HCP5
1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 7.6E-02
CUI: C0085655
Disease: Polymyositis
Polymyositis 		0.700 1.000 1 2016 2016
dbSNP: rs3094013
rs3094013
HCP5
1.000 0.080 6 31466589 non coding transcript exon variant G/A snv 7.6E-02
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3131643
rs3131643
HCP5
6 31475005 intron variant G/A snv 0.12
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs3131643
rs3131643
HCP5
6 31475005 intron variant G/A snv 0.12
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs3828889
rs3828889
HCP5 ; HCG26
1.000 0.080 6 31472874 intron variant T/C snv 0.79
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome 		0.700 1.000 1 2019 2019
dbSNP: rs75640364
rs75640364
HCP5
6 31465789 non coding transcript exon variant G/C snv 6.1E-02
CUI: C0019360
Disease: Herpes zoster disease
Herpes zoster disease 		0.700 1.000 1 2019 2019
dbSNP: rs79022003
rs79022003
HCP5
6 31465935 non coding transcript exon variant T/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9281492
rs9281492
HCP5
6 31473191 intron variant -/T delins 0.33
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs2395029
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs2395029
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 2 2009 2010
dbSNP: rs2395029
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0.800 1.000 2 2009 2019
dbSNP: rs2395029
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs2395029
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 2 2009 2010