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 InternationalCreative Commons License
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)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000264534 DNA arraySNP - - - 2 M. Hashim Raza


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