Variant #0000595098 (NC_000013.10:g.(?_46802668)_(53731757_?)?)
| Individual ID |
00263423 |
| Chromosome |
13 |
| Allele |
Parent #1 |
| 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.(?_46802668)_(53731757_?)? |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
13q14.12-q14.3 |
| DB-ID |
chr13_002259 |
| Variant remarks |
Linkage region flanked by SNPs rs625052 and rs1322938. This region was previously associated with NWR as well. |
| Reference |
Andres, 2019 under review |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
M. Hashim Raza |
| Database submission license |
Creative Commons Attribution-NonCommercial 4.0 International |
| Created by |
M. Hashim Raza |
| Date created |
2019-08-29 17:15:52 +02:00 (CEST) |
| Date last edited |
2019-08-30 11:46:12 +02:00 (CEST) |

Variant on transcripts
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