Variant #0000000991 (NC_000019.10:g.11116926C>T, NM_000527.4:c.1773C>T (LDLR))
Individual ID |
00000196 |
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.11116926C>T |
Published as |
c.1773T>C |
Reference |
dbSNP, ClinVar |
DB-ID |
LDLR_000020 See all 4 reported entries |
dbSNP ID |
rs688 |
Frequency |
19/40 |
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 |
2020-11-29 12:35:42 +08:00 (CST) |
Date last edited |
2021-08-24 15:38:34 +08:00 (CST) |

Variant on transcripts
Screenings
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