rs6180, GHR

N. diseases: 6
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.
Height
CUI: C0489786
Disease: Height
517 0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 0.700 1.000 1 2011 2011
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 0.010 1.000 1 2006 2006
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 0.010 1.000 1 2003 2003
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 0.010 1.000 1 2003 2003
Isolated somatotropin deficiency
CUI: C3714796
Disease: Isolated somatotropin deficiency
27 0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 0.010 1.000 1 2007 2007
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 0.010 1.000 1 2006 2006