Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 11:2160829 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM830002, CM074289

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 30 HGVS names - click the plus to show

About this variant

This variant overlaps 35 transcripts, is associated with 4 phenotypes and is mentioned in 3 citations.

Variation displays