Variant #0010160806 (NC_000017.10:g.6182C>T)

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.6182C>T
DB-ID -
dbSNP ID -
gnomAD frequency 5/147992
gnomAD homozygote count 0/73991
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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