Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:119025215 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 32 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variation displays