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/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 4:39031878 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2566092

This variation has 5 HGVS names - click the plus to show

Variation displays