Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 11:5225710 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM870012 ; PhenCode HbVar.485 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 6 transcripts, has 2 individual genotypes, is associated with 5 phenotypes and is mentioned in 7 citations.

Variation displays