We work in a non-profit research centre to find new genes, diseases and find new medication. since we have a lot of samples and data and everyone has their own way of storing them that creates an issue for us later. So I decided to create a database for our use however I still feel confused on how to organize it. so if anyone can help me that would be really awesome. here is the list of things we need in the database.

FirstName LastName Age Gender MaritalStatus Location ContactNumber FamilyID MRN ModeOfInheratense Disease StatusOfSubject FamilyID FamilyNumber Number Of Affected Members Pedigree Age of disease onset

SampleID
Location
GenePanel
WGA (Whole Genome Amplification)
CRP Labeling
Genetics Labeling
InHouseExom
Outsourced exom

Case Solved (Yes\No)
ExomID
ExomNumber
Spreadsheet of exome
Variant (Nucleotide Change ,Amino Acid Change)
Nucleotide Change
Amino Acid Change 
Name of the Gene
NewGene (Yes\No)
Mode of inheritance (Dominant\recessive\X-linked)




Cardiac Ultrasound
Other Medical condition
Referral Physician 
Followed by