Variant #0000972063 (NC_000004.11:g.6279400G>A, NM_006005.3:c.218G>A (WFS1))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6279400G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
WFS1_000943 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1730039692 |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2024-03-29 08:43:01 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|