Variant #0001029811 (NC_000006.11:g.40997833G>T)

Individual ID 00464366
Chromosome 6
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification association
DNA change (genomic) (Relative to hg19 / GRCh37) g.40997833G>T
DNA change (hg38) g.41030094G>T
Published as -
ISCN 6p21.1-p12.3
DB-ID chr6_008173
Variant remarks LOD score 1.92
Reference PMID:Yousaf 2024:39334596
ClinVar ID -
dbSNP ID rs736794
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Sahib Kaloti
Database submission license No license selected
Created by Sahib Kaloti
Date created 2025-03-07 23:21:07 +01:00 (CET)
Date last edited 2025-03-12 11:36:04 +01:00 (CET)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000466001 DNA arraySNP - - - 2 Sahib Kaloti


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