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Title : Genetic risk score - OMIM - NCBI
link : Genetic risk score - OMIM - NCBI

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.

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• Search OMIM for "Genetic risk score" 

601696 - NOVELTY SEEKING PERSONALITY TRAIT

RISK-TAKING BEHAVIOR, INCLUDED

Cytogenetic locations: 11p15.5

OMIM:

 

601696

Gene summaries Genetic tests Medical literature

Select item 6018472.

#601847 - CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 2; PFIC2

Cytogenetic locations: 2q31.1

OMIM:

 

601847

Gene summaries Genetic tests Medical literature

Select item 6139273.

*613927 - COMPLEMENT COMPONENT 2; C2

Cytogenetic locations: 6p21.33

OMIM:

 

613927

Gene summaries Genetic tests Medical literature

Select item 1384704.

*138470 - COMPLEMENT FACTOR B; CFB

Cytogenetic locations: 6p21.33

OMIM:

 

138470

Gene summaries Genetic tests Medical literature

Select item 1093505.

%109350 - GASTROESOPHAGEAL REFLUX; GER

Cytogenetic locations: 13q14

OMIM:

 

109350

Gene summaries Genetic tests Medical literature

Select item 1212006.

#121200 - SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1

EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED

Cytogenetic locations: 20q13.33

OMIM:

 

121200

Gene summaries Genetic tests Medical literature

Select item 6043707.

#604370 - BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1

BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1, INCLUDED

Cytogenetic locations: 17q21.31

OMIM:

 

604370

Gene summaries Genetic tests Medical literature

Select item 6124608.

#612460 - BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14; BMIQ14

Cytogenetic locations: 16q12.2

OMIM:

 

612460

Gene summaries Genetic tests Medical literature

Select item 1672509.

#167250 - PAGET DISEASE OF BONE 3; PDB3

Cytogenetic locations: 5q35.3

OMIM:

 

167250

Gene summaries Genetic tests Medical literature

Select item 61255510.

#612555 - BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2

BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2, INCLUDED

Cytogenetic locations: 13q13.1

OMIM:

 

612555

Gene summaries Genetic tests Medical literature

Select item 10378011.

#103780 - ALCOHOL DEPENDENCE

Cytogenetic locations: 4q23, 1pter-p36.13, 4p12, 1pter-p36.13, 13q14.2

OMIM:

 

103780

Gene summaries Genetic tests Medical literature

Select item 27330012.

#273300 - TESTICULAR GERM CELL TUMOR; TGCT

SEMINOMA, INCLUDED

Cytogenetic locations: 4q12, 1pter-p36.13, 19p13.3

OMIM:

 

273300

Gene summaries Genetic tests Medical literature

Select item 12620013.

#126200 - MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO; MS

MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 1, INCLUDED; MS1, INCLUDED

Cytogenetic locations: 6p21.32, 1pter-p36.13, 2q37.3

OMIM:

 

126200

Gene summaries Genetic tests Medical literature

Select item 20890014.

#208900 - ATAXIA-TELANGIECTASIA; AT

AT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED

Cytogenetic locations: 11q22.3

OMIM:

 

208900

Gene summaries Genetic tests Medical literature

Select item 25025015.

#250250 - CARTILAGE-HAIR HYPOPLASIA; CHH

Cytogenetic locations: 9p13.3

OMIM:

 

250250

Gene summaries Genetic tests Medical literature

Select item 60831816.

%608318 - CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 4

Cytogenetic locations: 14q32

OMIM:

 

608318

Gene summaries Genetic tests Medical literature

Select item 60626317.

%606263 - PAGET DISEASE OF BONE 4; PDB4

Cytogenetic locations: 5q31

OMIM:

 

606263

Gene summaries Genetic tests Medical literature

Select item 19068518.

#190685 - DOWN SYNDROME

DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED

Cytogenetic locations: 1pter-p36.13, 21q22.3

OMIM:

 

190685

Gene summaries Genetic tests Medical literature

Select item 61474219.

#614742 - PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1

Cytogenetic locations: 5p15.33

OMIM:

 

614742

Gene summaries Genetic tests Medical literature

Select item 15835020.

#158350 - COWDEN SYNDROME 1; CWS1

DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED

Cytogenetic locations: 10q23.31

OMIM:

 

158350

Gene summaries Genetic tests Medical literature

Thus Article Genetic risk score - OMIM - NCBI

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