Variant #0000000006 (NC_000001.10:g.12758_12759insC)

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.12758_12759insC
DB-ID -
dbSNP ID -
gnomAD frequency 1/12908
gnomAD homozygote count 0/6453
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
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
Options




Variant on transcripts

Stop! No variants on transcripts found!