ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xp11.22-11.21(chrX:52901458-55684871)x2
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 | |||
FGD1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
320 | 517 | |
IQSEC2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1140 | 1296 | |
KDM5C | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
716 | 881 | |
PHF8 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
193 | 342 | |
SMC1A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
900 | 1064 | |
HSD17B10 | No evidence available | No evidence available |
GRCh38 GRCh37 |
163 | 319 | |
HUWE1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
1280 | 1513 | |
ALAS2 | - | - |
GRCh38 GRCh37 |
195 | 396 | |
APEX2 | - | - |
GRCh38 GRCh37 |
26 | 157 | |
FAM104B | - | - | - |
GRCh38 GRCh37 |
- | 44 |
There are 24 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Sep 8, 2020 | RCV001834255.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022