Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.40 (A)
Location

Chromosome 19:45306777 (forward strand) | View in location tab

Co-located

with COSMIC COSM3766376 (A/G)

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 2 HGVS names - click the plus to show

This variant has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 4368 sample genotypes and is mentioned in 2 citations.

Variant displays