SAMN02184073
External Id
dbGaP
INSDC center name
2013-06-01T01:23:36.670Z
INSDC first public
2024-05-03T14:23:01.280Z
INSDC last update
SRS448008
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS448008
SRA accession
DNA
analyte type
NHGRI_AmishMennonite
biospecimen repository
26513
biospecimen repository sample id
Blood
http://purl.obolibrary.org/obo/UBERON_0000178
body site
phs000623
gap_accession
1
gap_consent_code
GRU
gap_consent_short_name
1020479
gap_sample_id
761972
gap_subject_id
SNP Genotypes (NGS)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Case Set
study design
Rare Mendelian Disease in Old Order Amish and Mennonite Patients
study name
26513
submitted sample id
26513
submitted subject id
NHGRI_AmishMennonite
submitter handle
DNA sample from Blood of a human female participant in the dbGaP study Rare Mendelian Disease in Old Order Amish and Mennonite Patients
title