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: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
Xeroderma Pigmentosum, Complementation Group D
0.010 1.000 1 2014 2014
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
0.010 1.000 1 2013 2013
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.010 1.000 1 2013 2013
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0750151
Disease: Vaso-Occlusive Crisis
Vaso-Occlusive Crisis
0.010 1.000 1 2018 2018
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
0.010 1.000 1 2017 2017
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
0.020 0.500 2 2008 2010
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss
0.010 1.000 1 2012 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 1.000 2 2010 2010
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
Stage IV Prostate Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
Stage IV Prostate Cancer AJCC v8
0.010 1.000 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
Stage IV Prostate Cancer AJCC v7
0.010 1.000 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease
0.010 1.000 1 2014 2014
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0855247
Disease: Sleep attack
Sleep attack
0.010 1.000 1 2019 2019
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2013 2013
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2013 2013
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0036572
Disease: Seizures
Seizures
0.010 1.000 1 2019 2019
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2012 2012
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2009 2009
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.100 0.857 14 2007 2016
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C1853195
Disease: Prostate Cancer, Hereditary, 7
Prostate Cancer, Hereditary, 7
0.010 1.000 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.080 0.875 8 2004 2017
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2008 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
0.010 1.000 1 2015 2015
dbSNP: rs4880
rs4880
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.010 1.000 1 2017 2017