Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.25 (A)
Location

Chromosome 20:766512 (forward strand) | View in location tab

Co-located

with dbSNP rs77339354 (G/T), rs77952806 (C/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59332899

This variation has 4 HGVS names - click the plus to show

Variation displays