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 11:47339757 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981326 ; PhenCode FHC0045 (C/T)

Most severe consequence
Clinical significance

Synonyms

Uniprot VAR_003918

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

Variation displays