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Public Profile -- huAA16BD

Public profile url: https://my.pgp-hms.org/profile/huAA16BD

Personal Health Records

Demographic Information

Date of Birth1927-11-17 (91 years old)
Gender
Weight
Height
Blood Type
Race

Conditions

Name Start Date End Date
exertional dyspnea
paresthesias feet
HYPERCHOLESTEROLEMIA
gerd
impaired glucose tolerance fasting
extreme myopia 1927-11-17
microphthalmia/anopthalmia congenital 1927-11-17
Anemia 2012-03-01
ASTHMA
Peripheral Neuropathy
Hypertension

Medications

Name Dosage Frequency Start Date End Date
Albuterol one puff tid prn wheezing
DILTIAZEM (ETHEX-ER) 240MG CAP,SA one p.o. daily
Lisinopril 40 Milligram per milliliter (mg/ml) Take 40, daily

Allergies

Name Reaction/Severity Start Date End Date
Amoxycillin allergy wheezing 2009-06-01

Procedures

Name Date

Test Results

Name Result Date

Immunizations

Name Date

Updated: 2012-05-26T11:31:53.0190852

Samples

None available.

Uploaded data

Date Data type Source Name Download Report
2017-09-10 Veritas Genetics Participant 55001508056937.vcf.gz Download
(498 MB)
2013-05-01 exome vcf file from 23andme pilot (reinterpreted) Participant huAA16BD_exome_sevenbridgesgenomics_vcf Download
(38 MB)
2012-05-26 23andMe Participant huAA16BD_23andme_SNPs Download
(8.06 MB)
View report
• female
• 986,380 positions covered
• ref. b36
2012-05-04 exome vcf file from 23andme pilot Participant huAA16BD_exome_23andme_pilot_vcf.gz Download
(6.82 MB)

Geographic Information

State:Pennsylvania
Zip code:16505

Family Members Enrolled

child linked 2012-05-23 19:39:34 UTC
not genetically related (e.g. husband/wife) linked 2012-05-23 19:39:37 UTC

Surveys

PGP Participant Survey Responses submitted 5/14/2012 15:14:22. Show responses
Timestamp 5/14/2012 15:14:22
Year of birth 80-89 years
Which statement best describes you? I am comfortable making my genome sequence data publicly available without prior review.
Severe disease or rare genetic trait Yes
Do you have a severe genetic disease or rare genetic trait? If so, you can add a description for your public profile. Microphalmia in my right eye My grandson was born blind.
Disease/trait: Onset Congenital / present at birth
Disease/trait: Rarity Uncommon
Disease/trait: Severity Moderate severity disease
Disease/trait: Relative enrollment Maybe
Disease/trait: Diagnosis Yes
Disease/trait: Genetic confirmation No
Disease/trait: Documentation No
Sex/Gender Female
Race/ethnicity White
Maternal grandmother: Country of origin United States
Paternal grandmother: Country of origin United States
Paternal grandfather: Country of origin United States
Maternal grandfather: Country of origin United States
Enrollment of relatives No
Enrollment of older individuals No
Enrollment of parents No
Have you uploaded genetic data to your PGP participant profile? No, but I have genetic data and plan to upload it
Have you used the PGP web interface to record a designated proxy? Yes
Have you uploaded health record data using our Google Health or Microsoft Healthvault interfaces? No, but I plan to
Blood sample Yes
Saliva sample Yes
Microbiome samples Yes
Tissue samples from surgery Yes
Tissue samples from autopsy Yes

Absolute Pitch Survey [see all responses]

Can tell if notes are in tune: Yes
Can sing a melody on key: No
Can recognize musical intervals: No
Do you have absolute pitch? No

Enrollment History

Participant ID:huAA16BD
Account created:2012-05-09 20:01:32 UTC
Eligibility screening:2012-05-09 20:12:54 UTC (passed v2)
Exam:2012-05-09 21:27:42 UTC (passed v20120430)
Consent:2015-08-06 14:32:03 UTC (passed v20150505)
Enrolled:2012-05-12 01:37:28 UTC