Variant #0011147394 (NC_000019.9:g.66044T>C)

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.66044T>C
DB-ID -
dbSNP ID -
gnomAD frequency 3/88
gnomAD homozygote count 1/42
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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