ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q26.2(chr10:127257925-127873894)x3
Germline
Classification
(1)
Likely benign
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
DOCK1 | - | - |
GRCh38 GRCh37 |
99 | 243 | |
FOXI2 | - | - |
GRCh38 GRCh37 |
33 | 123 | |
LOC126861089 | - | - | - | GRCh38 | - | 33 |
LOC130004946 | - | - | - | GRCh38 | - | 28 |
LOC130004947 | - | - | - | GRCh38 | - | 33 |
NPS | - | - |
GRCh38 GRCh37 |
4 | 93 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jul 18, 2014 | RCV000139873.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024