Original source

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

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

Chromosome 4:53431633 (forward strand) | View in location tab

Co-located

with dbSNP rs58637505 (C/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71621066

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

Variation displays