| attributes |
| gap_accession |
phs000553 |
| submitter handle |
Rare_Pediatric_Phenotypes |
| biospecimen repository |
Rare_Pediatric_Phenotypes |
| study name |
Familial Exome Sequencing in Rare Pediatric Phenotypes |
| study design |
Family/Twin/Trios |
| biospecimen repository sample id |
S1 |
| submitted sample id |
S1 |
| submitted subject id |
x1 |
| gap_sample_id |
915364 |
| gap_subject_id |
706658 |
| sex |
female |
| study disease |
Mendelian |
| body site |
Blood |
| histological type |
Whole blood leukocytes |
| analyte type |
DNA |
| is tumor |
No |
| subject is affected |
Yes |
| molecular data type |
SNP Genotypes (Array) |
| gap_consent_code |
1 |
| gap_consent_short_name |
GRU-MDS |
|