Variant #0012376996 (NC_000021.8:g.9825853G>C)

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.9825853G>C
DB-ID -
dbSNP ID rs767167835
gnomAD frequency 10/35994
gnomAD homozygote count 0/17979
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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