Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W
Location

Chromosome 5:132299399 (forward strand) | View in location tab

Co-located

with dbSNP rs61272303 (A/-/ATTT)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36128629

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

Variation displays