Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 4:73411994 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS880065

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB AnalbuminemiaVancouver

This variation has 24 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays