Original source

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

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

Chromosome 4:74277711 (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 20 HGVS names - click the plus to show

Genotyping chips

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

Variation displays