Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

Chromosome 2:219418537 (forward strand) | View in location tab

Co-located

with COSMIC COSM3757962 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 2509 individual genotypes and is associated with 2 phenotypes.

Variation displays