SAMN01906000
External Id
dbGaP
INSDC center name
2013-01-26T01:28:23.527Z
INSDC first public
2024-05-03T22:08:07.300Z
INSDC last update
SRS449757
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS449757
SRA accession
DNA
analyte type
Rare_Pediatric_Phenotypes
biospecimen repository
S3
http://www.ebi.ac.uk/efo/EFO_0002791
biospecimen repository sample id
Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs000553
gap_accession
1
gap_consent_code
GRU-MDS
gap_consent_short_name
915366
gap_sample_id
706660
gap_subject_id
Whole blood leukocytes
histological type
No
is tumor
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
Family/Twin/Trios
study design
Mendelian Randomization Analysis
study disease
Familial Exome Sequencing in Rare Pediatric Phenotypes
study name
Yes
subject is affected
S3
http://www.ebi.ac.uk/efo/EFO_0002791
submitted sample id
x3
submitted subject id
Rare_Pediatric_Phenotypes
submitter handle
Non-tumor DNA sample from Blood of a human female participant in the dbGaP study Familial Exome Sequencing in Rare Pediatric Phenotypes
title