ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q26.3(chr15:101734079-102429112)x3
Germline
Classification
(1)
Likely benign
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 | |||
CHSY1 | - | - |
GRCh38 GRCh37 |
182 | 322 | |
OR4F15 | - | - | - |
GRCh38 GRCh37 |
22 | 97 |
OR4F6 | - | - | - |
GRCh38 GRCh37 |
19 | 103 |
PCSK6 | - | - |
GRCh38 GRCh37 |
16 | 114 | |
SELENOS | - | - |
GRCh38 GRCh37 |
16 | 110 | |
SNRPA1 | - | - |
GRCh38 GRCh37 |
9 | 100 | |
TARS3 | - | - | - |
GRCh38 GRCh37 |
51 | 158 |
TM2D3 | - | - |
GRCh38 GRCh37 |
16 | 122 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 1, 2021 | RCV000683736.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022