Original source

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

Alleles
T/C | Ambiguity code: Y | MAF: 0.38 (C)
Location

Chromosome 12:52316099 (forward strand) | View in location tab

Co-located

with COSMIC COSM147521 (T/C)

Most severe consequence
 
Synonymous variant
Evidence status

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays