Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 12:111803962 (forward strand) | View in location tab

Co-located

with COSMIC COSM147611 (G/A) ; HGMD-PUBLIC CM870003

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3473 individual genotypes, is associated with 19 phenotypes and is mentioned in 49 citations.

Variation displays