Genomic variant #0000000257

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.23745865C>T
Reference dbSNP
DB-ID chr1_000001 See all 10 reported entries
Frequency 0.924 Control
Allele Count 658
Allele Number 712
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000003 DNA TaqMan - 253 Admin