ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q26.3(chr15:100853021-102429112)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 | |||
ADAMTS17 | - | - |
GRCh38 GRCh37 |
1209 | 1323 | |
ALDH1A3 | - | - |
GRCh38 GRCh37 |
36 | 226 | |
ASB7 | - | - |
GRCh38 GRCh37 |
14 | 111 | |
CERS3 | - | - |
GRCh38 GRCh37 |
85 | 203 | |
CHSY1 | - | - |
GRCh38 GRCh37 |
190 | 332 | |
LINS1 | - | - |
GRCh38 GRCh37 |
184 | 283 | |
LRRK1 | - | - |
GRCh38 GRCh37 |
756 | 901 | |
OR4F15 | - | - | - |
GRCh38 GRCh37 |
23 | 99 |
OR4F6 | - | - | - |
GRCh38 GRCh37 |
21 | 106 |
PCSK6 | - | - |
GRCh38 GRCh37 |
16 | 115 |
There are 4 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) |
|
Dec 16, 2021 | RCV001259829.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022