rs1801725, CASR

N. diseases: 39
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Calcium level result
CUI: C0428302
Disease: Calcium level result
51 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.700 1.000 3 2010 2013
Calcium measurement
CUI: C0201925
Disease: Calcium measurement
71 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.800 1.000 4 2010 2018
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.020 1.000 2 2008 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.020 0.500 2 2007 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2016 2016
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2019 2019
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.020 1.000 2 2018 2019
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.020 1.000 2 2018 2019
Hypercalcemia
CUI: C0020437
Disease: Hypercalcemia
9 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2009 2009
Hyperparathyroidism
CUI: C0020502
Disease: Hyperparathyroidism
14 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2016 2016
HYPERPARATHYROIDISM, NEONATAL SEVERE
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
14 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2007 2007
Hyperparathyroidism, Primary
CUI: C0221002
Disease: Hyperparathyroidism, Primary
39 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.060 0.667 6 2001 2018
Hyperparathyroidism, Secondary
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
4 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2015 2015
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2018 2018
Lactose Intolerance
CUI: C0022951
Disease: Lactose Intolerance
2 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2008 2008
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2017 2017
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.020 0.500 2 2008 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.020 1.000 2 2010 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 0.010 1.000 1 2018 2018