This variant has been flagged

None of the variant alleles match the reference allele (T)

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: T|Ambiguity code: R
Note: The reference base for this variant (A) does not match the Ensembl reference base (T) at this location.
Location

Chromosome 16:20336704 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 10 transcripts and has 268 sample genotypes.

Variant displays