ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q22.31(chr15:64978681-65679053)
Germline
Classification
(1)
Uncertain significance
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 | |||
ANKDD1A | - | - | - |
GRCh38 GRCh37 |
42 | 61 |
CILP | - | - |
GRCh38 GRCh37 |
108 | 123 | |
CLPX | - | - |
GRCh38 GRCh37 |
98 | 113 | |
IGDCC3 | - | - |
GRCh38 GRCh37 |
52 | 67 | |
IGDCC4 | - | - |
GRCh38 GRCh37 |
90 | 104 | |
KBTBD13 | - | - |
GRCh38 GRCh37 |
588 | 603 | |
MTFMT | - | - |
GRCh38 GRCh37 |
228 | 262 | |
OAZ2 | - | - |
GRCh38 GRCh37 |
- | 15 | |
PARP16 | - | - | - |
GRCh38 GRCh37 |
22 | 37 |
PDCD7 | - | - |
GRCh38 GRCh37 |
19 | 48 |
There are 8 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 1, 2022 | RCV002052484.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022