Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
 
Splice acceptor variant
Evidence status

Clinical significance

Synonyms

LSDB AnalbuminemiaVancouver

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

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 34 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays