Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 11:32392032 (forward strand) | View in location tab

Co-located

with COSMIC COSM3397637 (G/A), COSM21397 (G/A) ; HGMD-PUBLIC CM971596

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14632, 18533

This variation has 19 HGVS names - click the plus to show

Variation displays