SAMN29548334
External Id
dbGaP
INSDC center name
2022-07-06T22:08:14.200Z
INSDC first public
2022-10-21T22:07:17.840Z
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
S1018
biospecimen repository sample id
Blood
body site
phs001517
gap_accession
1
gap_consent_code
DS-ED-NPU-GSO
gap_consent_short_name
5056276
gap_sample_id
4055409
gap_subject_id
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
sex
Case Set
study design
Retinitis Pigmentosa
study disease
Genetics of Human Inherited Retinal Diseases (GHIRD)
study name
Yes
subject is affected
S1018
submitted sample id
1018
submitted subject id
NEI Inherited Retinal Diseases
submitter handle
DNA sample from Blood of a human female participant in the dbGaP study Genetics of Human Inherited Retinal Diseases (GHIRD)
title