ClinVar Genomic variation as it relates to human health
NM_001072.4(UGT1A6):c.862-10037A>G
Germline
Classification
(1)
Likely benign
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 | |||
UGT1A | - | - | - | GRCh38 | - | 548 |
UGT1A1 | - | - |
GRCh38 GRCh37 |
1 | 351 | |
UGT1A10 | - | - |
GRCh38 GRCh37 |
- | 554 | |
UGT1A3 | - | - |
GRCh38 GRCh37 |
- | 374 | |
UGT1A4 | - | - |
GRCh38 GRCh37 |
- | 399 | |
UGT1A5 | - | - |
GRCh38 GRCh37 |
- | 417 | |
UGT1A6 | - | - |
GRCh38 GRCh37 |
- | 457 | |
UGT1A7 | - | - |
GRCh38 GRCh37 |
- | 508 | |
UGT1A8 | - | - |
GRCh38 GRCh37 |
- | 577 | |
UGT1A9 | - | - |
GRCh38 GRCh37 |
- | 536 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Sep 21, 2021 | RCV004540937.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 12, 2024