Variant #0000879755 (NC_000016.9:g.(28578529_16_2883343)_(29042109_29678569)dup)
Individual ID |
00418361 |
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
association |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(28578529_16_2883343)_(29042109_29678569)dup |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
chr16_006622 |
Variant remarks |
variant not maternally inherited; associated with increased risk of being underweight and having reduced head circumference |
Reference |
PubMed: Scott 2017 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline/De novo (untested) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2022-09-28 19:55:25 +02:00 (CEST) |
Date last edited |
N/A |
Variant on transcripts
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