Original source

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

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

Chromosome 9:711728 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_048299

This variation has 9 HGVS names - click the plus to show

Variation displays