ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6q21(chr6:108992778-110303422)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
AK9 | - | - |
GRCh38 GRCh37 |
83 | 137 | |
ARMC2 | - | - |
GRCh38 GRCh37 |
57 | 98 | |
CD164 | - | - |
GRCh38 GRCh37 |
90 | 122 | |
CEP57L1 | - | - | - |
GRCh38 GRCh37 |
30 | 50 |
FIG4 | - | - |
GRCh38 GRCh37 |
982 | 1018 | |
FOXO3 | - | - |
GRCh38 GRCh37 |
40 | 65 | |
GPR6 | - | - |
GRCh38 GRCh37 |
23 | 48 | |
MICAL1 | - | - |
GRCh38 GRCh37 |
1004 | 1057 | |
PPIL6 | - | - | - |
GRCh38 GRCh37 |
25 | 53 |
SESN1 | - | - |
GRCh38 GRCh37 |
- | 39 |
There are 2 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
- | RCV003986671.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 30, 2024