ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17p13.1(chr17:6934163-8217978)x1
Germline
Classification
(1)
drug response
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 | |||
TP53 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
3211 | 3306 | |
KDM6B | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
402 | 502 | |
ACADVL | - | - |
GRCh38 GRCh37 |
1704 | 1909 | |
ACAP1 | - | - |
GRCh38 GRCh38 GRCh37 |
27 | 59 | |
ALOX12B | - | - |
GRCh38 GRCh37 |
291 | 344 | |
ALOX15B | - | - |
GRCh38 GRCh37 |
40 | 72 | |
ALOXE3 | - | - |
GRCh38 GRCh37 |
196 | 271 | |
ARHGEF15 | - | - |
GRCh38 GRCh37 |
571 | 598 | |
ASGR1 | - | - |
GRCh38 GRCh37 |
9 | 38 | |
ASGR2 | - | - |
GRCh38 GRCh37 |
15 | 42 |
There are 67 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
drug response (1) |
|
Nov 27, 2017 | RCV000626431.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023