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: A | Ambiguity code: W
Location

Chromosome 18:5405833 (forward strand) | View in location tab

Most severe consequence

This variation has 19 HGVS names - click the plus to show

Variation displays