Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.40 (C)
Location

Chromosome 2:44039875 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56883360

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

This variation has assays on 8 chips - click the plus to show

Variation displays