ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3q11.2-12.1(chr3:97606054-98499715)x3
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 | |||
CLDND1 | - | - |
GRCh38 GRCh37 |
17 | 30 | |
CPOX | - | - |
GRCh38 GRCh37 |
189 | 287 | |
CRYBG3 | - | - | - |
GRCh38 GRCh37 |
11 | 36 |
GABRR3 | - | - |
GRCh38 GRCh37 |
36 | 60 | |
GPR15 | - | - |
GRCh38 GRCh37 |
26 | 39 | |
OR5AC2 | - | - | - |
GRCh38 GRCh37 |
27 | 46 |
OR5H1 | - | - | - |
GRCh38 GRCh37 |
33 | 52 |
OR5H14 | - | - | - |
GRCh38 GRCh37 |
29 | 48 |
OR5H15 | - | - | - |
GRCh38 GRCh37 |
28 | 47 |
OR5H2 | - | - | - |
GRCh38 GRCh37 |
17 | 36 |
There are 7 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 23, 2019 | RCV001005456.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022