ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q36.1-36.3(chr7:151104277-159325876)x3
Germline
Classification
(1)
Pathogenic
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 | |||
KMT2C | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1592 | 1736 | |
MNX1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
231 | 400 | |
SHH | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
334 | 571 | |
DPP6 | Little evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 |
251 | 300 | |
RNF32 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
8 | 112 | |
DNAJB6 | No evidence available | No evidence available |
GRCh38 GRCh37 |
439 | 530 | |
EN2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
30 | 113 | |
PRKAG2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
1116 | 1291 | |
ABCF2 | - | - |
GRCh38 GRCh37 |
- | 90 | |
ABCF2-H2BK1 | - | - | - | GRCh38 | - | 47 |
There are 307 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 |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Dec 22, 2010 | RCV000136683.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024