Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 11:47448832 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073304

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10270

This variation has 18 HGVS names - click the plus to show

Variation displays