Variant #0000000075 (NC_000001.10:g.17408C>G)

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.17408C>G
DB-ID -
dbSNP ID rs747093451
gnomAD frequency 444/67058
gnomAD homozygote count 0/33085
Average frequency (gnomAD v.2.1.1) 0.00662 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!