SAMN01798267
External Id
dbGaP
INSDC center name
2012-11-02T18:46:54.340Z
INSDC first public
2024-05-03T21:27:26.853Z
INSDC last update
SRS375869
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS375869
SRA accession
DNA
analyte type
NHGRI Mendelian Familial Hyperlipidemia
biospecimen repository
291
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
880427
gap_sample_id
697412
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
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Mendelian
study design
Hyperlipidemia, Familial Combined
study disease
Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
study name
Yes
subject is affected
291
submitted sample id
291
submitted subject id
NHGRI Mendelian Familial Hyperlipidemia
submitter handle
DNA sample from ARM of a human female participant in the dbGaP study Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
title