Variant #0011167921 (NC_000019.9:g.1036699C>T, NM_019112.3:c.-3634C>T (ABCA7))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.1036699C>T
DB-ID -
dbSNP ID rs778284807
gnomAD frequency 3/151996
gnomAD homozygote count 0/75980
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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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 ./. c.-3634C>T r.(=) p.(=)