SAMN01798262
External Id
dbGaP
INSDC center name
2012-11-02T18:46:52.577Z
INSDC first public
2024-05-03T21:27:25.010Z
INSDC last update
SRS375863
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS375863
SRA accession
DNA
analyte type
NHGRI Mendelian Familial Hyperlipidemia
biospecimen repository
294
biospecimen repository sample id
ARM
http://purl.obolibrary.org/obo/UBERON_0001499
body site
phs000538
gap_accession
2
gap_consent_code
HD
gap_consent_short_name
880430
gap_sample_id
697415
gap_subject_id
BLOOD
http://purl.obolibrary.org/obo/UBERON_0000178
histological type
SNP Genotypes (NGS)
molecular data type
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
male
http://purl.obolibrary.org/obo/PATO_0000384
sex
Mendelian
study design
Hyperlipidemia, Familial Combined
study disease
Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
study name
Yes
subject is affected
294
submitted sample id
294
submitted subject id
NHGRI Mendelian Familial Hyperlipidemia
submitter handle
DNA sample from ARM of a human male participant in the dbGaP study Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
title