Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:44313579 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs454637

This variation has 2 HGVS names - click the plus to show

Variation displays