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 11:119028223 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 30 transcripts, is associated with 4 phenotypes and is mentioned in 5 citations.

Variant displays