Original source

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

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

Chromosome 11:5225488 (forward strand) | View in location tab


with HGMD-PUBLIC CR850010, CR045224, CR014260 ; PhenCode HbVar.968 (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

About this variant

This variant overlaps 11 transcripts, is associated with 2 phenotypes and is mentioned in 6 citations.

Variation displays