Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 6:32551937 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs35898212, rs28724090

This variation has 6 HGVS names - click the plus to show

Variation displays