SAMN29548336
External Id
dbGaP
INSDC center name
2022-07-06T22:08:14.283Z
INSDC first public
2022-10-21T22:07:17.920Z
INSDC last update
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
DNA
analyte type
NEI Inherited Retinal Diseases
biospecimen repository
S1027
biospecimen repository sample id
Blood
body site
phs001517
gap_accession
1
gap_consent_code
DS-ED-NPU-GSO
gap_consent_short_name
5056285
gap_sample_id
4055418
gap_subject_id
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
Case Set
study design
Retinitis Pigmentosa
study disease
Genetics of Human Inherited Retinal Diseases (GHIRD)
study name
Yes
subject is affected
S1027
submitted sample id
1027
submitted subject id
NEI Inherited Retinal Diseases
submitter handle
DNA sample from Blood of a human participant in the dbGaP study Genetics of Human Inherited Retinal Diseases (GHIRD)
title