SAMN01981784
External Id
dbGaP
INSDC center name
2013-03-18T02:37:07.090Z
INSDC first public
2024-05-09T00:47:16.057Z
INSDC last update
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
ERS19651192
SRA accession
DNA
analyte type
CIDR
biospecimen repository
M7896641
biospecimen repository sample id
Cell Line
http://purl.obolibrary.org/obo/CL_0000010
body site
phs000421
gap_accession
2
gap_consent_code
GRU
gap_consent_short_name
6953
gap_sample_id
54783
gap_subject_id
Cell Line
http://purl.obolibrary.org/obo/CL_0000010
histological type
No
is tumor
SNP Genotypes (imputed)
molecular data type
SNP Genotypes (Array)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Case-Control
study design
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
study name
M7896641
submitted sample id
4847
submitted subject id
CIDR
submitter handle
Non-tumor DNA sample from Cell Line of a human female participant in the dbGaP study A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
title