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: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis
0.720 1.000 2 2015 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 2 2016 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2013 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 1.000 2 2013 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 1.000 2 2013 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
Secondary malignant neoplasm of colon and/or rectum
0.010 1.000 1 2016 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.010 1.000 1 2018 2018
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0023529
Disease: Leukomalacia, Periventricular
Leukomalacia, Periventricular
0.010 1.000 1 2014 2014
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia
0.010 1.000 1 2013 2013
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2017 2017
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2012 2012
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2016 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014