domingo, 14 de enero de 2018

Genetic risk score - OMIM - NCBI

Genetic risk score - OMIM - NCBI





From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.



RISK-TAKING BEHAVIOR, INCLUDED
Cytogenetic locations: 11p15.5
3.
4.
5.
6.
EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED
Cytogenetic locations: 20q13.33
7.
BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1, INCLUDED
Cytogenetic locations: 17q21.31
9.
10.
BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2, INCLUDED
Cytogenetic locations: 13q13.1
11.
Cytogenetic locations: 4q23, 1pter-p36.13, 4p12, 1pter-p36.13, 13q14.2
12.
SEMINOMA, INCLUDED
Cytogenetic locations: 4q12, 1pter-p36.13, 19p13.3
13.
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 1, INCLUDED; MS1, INCLUDED
Cytogenetic locations: 6p21.32, 1pter-p36.13, 2q37.3
14.
AT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED
Cytogenetic locations: 11q22.3
15.
17.
18.
DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED
Cytogenetic locations: 1pter-p36.13, 21q22.3
20.
DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED
Cytogenetic locations: 10q23.31

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