This variation has been flagged

Flagged as suspect by dbSNP

Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/T | Ancestral: T | Ambiguity code: W
Location

Chromosome 6:161122165 (forward strand) | View in location tab

Most severe consequence
HGVS name

6:g.161122165A>T

Variation displays