ClinVar Genomic variation as it relates to human health
GRCh37/hg19 1p35.1(chr1:32608682-32953541)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
BSDC1 | - | - |
GRCh38 GRCh37 |
28 | 40 | |
CCDC28B | - | - |
GRCh38 GRCh37 |
21 | 35 | |
DCDC2B | - | - | - |
GRCh38 GRCh37 |
25 | 44 |
EIF3I | - | - |
GRCh38 GRCh37 |
7 | 21 | |
FAM167B | - | - | - |
GRCh38 GRCh37 |
8 | 27 |
FAM229A | - | - | - |
GRCh38 GRCh37 |
5 | 23 |
HDAC1 | - | - |
GRCh38 GRCh37 |
16 | 28 | |
IQCC | - | - | - |
GRCh38 GRCh37 |
35 | 51 |
KPNA6 | - | - |
GRCh38 GRCh37 |
11 | 25 | |
LCK | - | - |
GRCh38 GRCh37 |
247 | 261 |
There are 5 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) |
|
Apr 24, 2018 | RCV000684559.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022