rs138213197, HOXB13

N. diseases: 8
Source: CURATED ×
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.
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
374 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.800 0.938 1 2012 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
281 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.800 0.935 0 2012 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1390 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.720 0.500 0 2012 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.700 1.000 26 1996 2017
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
78 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
416 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
Prostate Cancer, Hereditary, 9
CUI: C1970250
Disease: Prostate Cancer, Hereditary, 9
1 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
PROSTATE CANCER, SUSCEPTIBILITY TO
CUI: C3469524
Disease: PROSTATE CANCER, SUSCEPTIBILITY TO
6 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0