Locus Specific Mutation Databases

Information If you know of an LSDB, which is not included in this list, you can submit it here.

  Please select the first letter of the Gene:
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Or, specify the HGNC Gene Symbol:

 Supported by:
Genome Scan, Next Generation Sequencing Services
Information Currently active filter: LSDBs for gene PHYH. Remove filter

8 entries on 1 page. Showing entries 1 - 8.

Database name     
Curators     
Unique variants     
Linked diseases     
Software     
Last updated     
Global Variome shared LOVD
https://databases.lovd.nl/shared/genes/PHYH		 LOVD-team, but with Curator vacancy
LUMC		 - - LOVD 3.X 2018-03-23
LOVD - Leiden Open Variation Database
Does not accept submissions
http://proteomics.bio21.unimelb.edu.au/lovd/genes/PHYH		 Graham Taylor
University of Melbourne		 - - LOVD 3.X 2013-06-13
ClinVar at NCBI
https://www.ncbi.nlm.nih.gov/clinvar/?term=PHYH[gene]
- - Other 2014-06-02
NDDVD - Neurodegenerative Diseases Variation Database
http://bioinf.suda.edu.cn/NDDvarbase/LOVDv.3.0/genes/PHYH		 Y Yang
SUDA		 - - LOVD 3.X 2015-10-23
BIPMed SNP Array
http://bipmed.iqm.unicamp.br/snparray/genes/PHYH		 Admin
BRAINN		 - - LOVD 3.X 2017-10-26
BIPMed SNP Array - HG19
http://bipmed.iqm.unicamp.br/snparray_hg19/genes/PHYH		 Admin
BRAINN		 - - LOVD 3.X 2018-10-01
BIPMed SNP Array - HG38
http://bipmed.iqm.unicamp.br/snparray_296/genes/PHYH		 Admin
BRAINN		 - - LOVD 3.X 2018-10-04
BIPMed WES - HG19
http://bipmed.iqm.unicamp.br/wes_hg19/genes/PHYH		 Admin
BRAINN		 - - LOVD 3.X 2018-12-08