Variant #0000001439 (NC_000012.12:g.4370383G>A, NM_020638.2:c.716C>T (FGF23))
Individual ID |
00000297 |
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.4370383G>A |
Published as |
- |
Reference |
dbSNP, ClinVar |
DB-ID |
FGF23_000001 |
dbSNP ID |
rs7955866 |
Frequency |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-12-24 14:26:43 +08:00 (CST) |
Date last edited |
2021-08-29 12:11:33 +08:00 (CST) |

Variant on transcripts
Screenings
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