Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.28 (A)
Location

Chromosome 19:33387931 (forward strand) | View in location tab

Co-located

with COSMIC COSM3756628 (G/A)

Most severe consequence
Evidence status

This variation has 7 synonyms - click the plus to show

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

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2848 individual genotypes and is mentioned in 1 citation.

Variation displays