Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

Chromosome 11:17461778 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM072824

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 21 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays