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: rs56388170
rs56388170
CREB5
7 28684757 intron variant G/T snv 0.37
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 3 2016 2019
dbSNP: rs1011384
rs1011384
CREB5
1.000 0.040 7 28472597 intron variant G/A snv 0.81
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10226517
rs10226517
CREB5
7 28712170 intron variant G/A snv 0.45
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs11976006
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.700 1.000 1 2019 2019
dbSNP: rs11976006
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11976006
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2019 2019
dbSNP: rs12700906
rs12700906
CREB5
7 28803353 intron variant T/C snv 0.29
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs160335
rs160335
CREB5
0.925 0.040 7 28548199 intron variant A/G snv 0.88
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2019 2019
dbSNP: rs160335
rs160335
CREB5
0.925 0.040 7 28548199 intron variant A/G snv 0.88
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs160354
rs160354
CREB5
7 28571847 intron variant C/A;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs17156577
rs17156577
CREB5
1.000 0.080 7 28317270 intron variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs177574
rs177574
CREB5
1.000 0.040 7 28455423 intron variant G/A snv 0.82
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs177576
rs177576
CREB5
1.000 0.040 7 28457489 intron variant C/T snv 0.68
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs177578
rs177578
CREB5
1.000 0.040 7 28458091 intron variant G/A snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1859020
rs1859020
CREB5
1.000 0.040 7 28468618 intron variant G/A snv 0.65
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs217514
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs217514
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2019 2019
dbSNP: rs217514
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs217514
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2019 2019
dbSNP: rs217514
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27
CUI: C0376705
Disease: Viral Load result
Viral Load result 		0.700 1.000 1 2019 2019
dbSNP: rs28531809
rs28531809
CREB5
7 28764294 intron variant T/A;C snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs56388170
rs56388170
CREB5
7 28684757 intron variant G/T snv 0.37
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs56388170
rs56388170
CREB5
7 28684757 intron variant G/T snv 0.37
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs56388170
rs56388170
CREB5
7 28684757 intron variant G/T snv 0.37
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs56388170
rs56388170
CREB5
7 28684757 intron variant G/T snv 0.37
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016