ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17q21.31(chr17:41464491-41835873)x3
Germline
Classification
(1)
Likely benign
criteria provided, single submitter
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 | |||
ARL4D | - | - |
GRCh38 GRCh37 |
10 | 31 | |
DHX8 | - | - |
GRCh38 GRCh37 |
39 | 106 | |
ETV4 | - | - |
GRCh38 GRCh37 |
22 | 87 | |
MEOX1 | - | - |
GRCh38 GRCh37 |
99 | 119 | |
SOST | - | - |
GRCh38 GRCh37 |
88 | 107 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Feb 14, 2018 | RCV000659194.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023