ClinVar Genomic variation as it relates to human health
GRCh38/hg38 4p15.31(chr4:19186844-20838471)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 | |||
KCNIP4 | - | - |
GRCh38 GRCh38 GRCh37 |
9 | 56 | |
LOC105374511 | - | - | - | GRCh38 | - | 17 |
LOC123477711 | - | - | - | GRCh38 | - | 14 |
LOC126806996 | - | - | - | GRCh38 | - | 17 |
LOC126806997 | - | - | - | GRCh38 | - | 17 |
LOC129992319 | - | - | - | GRCh38 | - | 14 |
LOC129992320 | - | - | - | GRCh38 | - | 14 |
LOC129992321 | - | - | - | GRCh38 | - | 14 |
LOC132089111 | - | - | - | GRCh38 | - | 16 |
LOC132089112 | - | - | - | GRCh38 | - | 16 |
There are 5 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 2, 2013 | RCV000141949.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024