Variant #0000000993 (NC_000019.10:g.11108701G>T, NC_000019.10(NM_000527.4):c.940+1187G>T (LDLR))
Individual ID |
00000197 |
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.11108701G>T |
Published as |
- |
Reference |
Livy Alex et al. (2012), dbSNP |
DB-ID |
LDLR_000035 |
dbSNP ID |
rs61318752 |
Frequency |
1/2 |
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 16:25:12 +08:00 (CST) |
Date last edited |
2021-08-24 15:39:59 +08:00 (CST) |

Variant on transcripts
Screenings
|
|