Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:2181113 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM082900

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_063739

This variation has 12 HGVS names - click the plus to show

Variation displays