SAMN01980869
External Id
dbGaP
INSDC center name
2013-03-18T02:35:01.477Z
INSDC first public
2024-04-19T17:21:52.957Z
INSDC last update
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
ERS19056715
SRA accession
CIDR
biospecimen repository
CIDR_18913@1061300226
biospecimen repository sample id
phs000421
gap_accession
0
gap_consent_code
926863
gap_sample_id
46835
gap_subject_id
SNP Genotypes (Array)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Case-Control
study design
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
study name
CIDR_18913@1061300226
submitted sample id
NA18913
http://purl.obolibrary.org/obo/CL_0000895
submitted subject id
CIDR
submitter handle
Sample from a human male participant in the dbGaP study A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
title