ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17q12(chr17:33073917-33863479)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
RAD51D | Some evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
32 | 1802 | |
CCT6B | - | - |
GRCh38 GRCh37 |
29 | 41 | |
FNDC8 | - | - | - |
GRCh38 GRCh37 |
18 | 40 |
LIG3 | - | - |
GRCh38 GRCh37 |
98 | 109 | |
NLE1 | - | - | - |
GRCh38 GRCh37 |
29 | 50 |
RFFL | - | - |
GRCh38 GRCh37 |
- | 31 | |
SLC35G3 | - | - | - |
GRCh38 GRCh37 |
34 | 47 |
SLFN11 | - | - |
GRCh38 GRCh37 |
71 | 87 | |
SLFN12 | - | - |
GRCh38 GRCh37 |
35 | 53 | |
SLFN12L | - | - |
GRCh38 GRCh37 |
28 | 42 |
There are 4 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 15, 2018 | RCV001006894.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023