ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Xp11.22-11.21(chrX:51664377-58055036)x3
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 | 516 | |
IQSEC2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1140 | 1296 | |
KDM5C | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
714 | 879 | |
PHF8 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
193 | 342 | |
SMC1A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
898 | 1062 | |
HSD17B10 | No evidence available | No evidence available |
GRCh38 GRCh37 |
162 | 318 | |
HUWE1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
1276 | 1509 | |
KLF8 | No evidence available | No evidence available |
GRCh38 GRCh37 |
29 | 159 | |
ALAS2 | - | - |
GRCh38 GRCh37 |
194 | 395 | |
APEX2 | - | - |
GRCh38 GRCh37 |
26 | 157 |
There are 154 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 |
---|---|---|---|---|
Pathogenic (1) |
|
Aug 12, 2011 | RCV000052392.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024