ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q26.3(chr10:132852693-134505024)x3
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 | |||
BNIP3 | - | - |
GRCh38 GRCh37 |
4 | 115 | |
DPYSL4 | - | - |
GRCh38 GRCh37 |
39 | 140 | |
INPP5A | - | - |
GRCh38 GRCh37 |
25 | 139 | |
JAKMIP3 | - | - |
GRCh38 GRCh37 |
58 | 161 | |
LINC02870 | - | - | - |
GRCh38 GRCh37 |
2 | 107 |
LRRC27 | - | - | - |
GRCh38 GRCh37 |
45 | 151 |
PPP2R2D | - | - |
GRCh38 GRCh37 |
4 | 119 | |
PWWP2B | - | - | - |
GRCh38 GRCh37 |
56 | 163 |
STK32C | - | - | - |
GRCh38 GRCh37 |
28 | 131 |
TCERG1L | - | - |
GRCh38 GRCh37 |
46 | 150 |
There is 1 more gene 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) |
|
Feb 8, 2023 | RCV003484824.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024