Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.20 (C)
Location

Chromosome 4:54248276 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61524375

This variation has 10 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays