Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.35 (A)
Location

Chromosome 16:20357398 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59332954

This variation has 7 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays