Genomic variant #0000000254

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.23757159T>C
Reference dbSNP
DB-ID chr1_000005 See all 7 reported entries
Frequency 0.230 Control
Allele Count 157
Allele Number 684
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