Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:2160835 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM082896

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_063729

This variation has 15 HGVS names - click the plus to show

Variation displays