Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 6:32584233 (forward strand) | View in location tab

Co-located

with dbSNP rs1059349 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs28724094

This variation has 3 HGVS names - click the plus to show

Variation displays