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 12:110919145 (forward strand) | View in location tab

Co-located

with COSMIC COSM4038693 (A/C) ; HGMD-PUBLIC CM981331 ; PhenCode FHC0202 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

About this variant

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

Variation displays