Variant #0000000539 (NC_000016.9:g.3297166G>C, NM_000243.2:c.1437C>G (MEFV))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3297166G>C |
| Reference |
https://www.ncbi.nlm.nih.gov/clinvar/variation/495755/ |
| DB-ID |
MEFV_000016 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| Owner |
Florian Bayersdorfer |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Florian Bayersdorfer |
| Date created |
2024-05-07 13:52:14 +00:00 (UTC) |
| Date last edited |
2025-07-29 10:43:24 +00:00 (UTC) |

Variant on transcripts
|
|