Genomic variant #0000000029

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.4592223C>T
Reference -
DB-ID chr1_000143 See all 2 reported entries
dbSNP ID rs17349020
Frequency 0.1912
Homozygous 44
Heterozygote 42
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin