Original source

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

Alleles
A/T | Ambiguity code: W
Location

Chromosome 12:33011045 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61534240

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

Variation displays