Variant #0012376983 (NC_000021.8:g.9825840C>T)

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.9825840C>T
DB-ID -
dbSNP ID rs770256152
gnomAD frequency 7/30578
gnomAD homozygote count 0/15276
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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