SAMN01981612
External Id
dbGaP
INSDC center name
2013-03-18T02:36:51.450Z
INSDC first public
2024-05-09T00:44:34.367Z
INSDC last update
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
ERS19651020
SRA accession
DNA
analyte type
CIDR
biospecimen repository
74133512
biospecimen repository sample id
Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs000421
gap_accession
2
gap_consent_code
GRU
gap_consent_short_name
5534
gap_sample_id
55122
gap_subject_id
Lymphyblastoid cell line
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
74133512
submitted sample id
5415
submitted subject id
CIDR
submitter handle
Non-tumor DNA sample from Blood of a human female participant in the dbGaP study A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
title