ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3p25.2(chr3:12487565-12997325)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 | |||
RAF1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
1060 | 1114 | |
CAND2 | - | - |
GRCh38 GRCh37 |
73 | 100 | |
IQSEC1 | - | - |
GRCh38 GRCh37 |
125 | 145 | |
LINC02022 | - | - | - | GRCh38 | - | 9 |
LOC121009641 | - | - | - | GRCh38 | - | 9 |
LOC126806607 | - | - | - | GRCh38 | - | 9 |
LOC129389024 | - | - | - | GRCh38 | - | 13 |
LOC129936172 | - | - | - | GRCh38 | - | 11 |
LOC129936173 | - | - | - | GRCh38 | - | 11 |
LOC129936174 | - | - | - | GRCh38 | - | 11 |
There are 34 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 16, 2011 | RCV000138028.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023