Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 20:46735184 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs16991780, rs3171155

This variation has 2 HGVS names - click the plus to show

Variation displays