Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.12 (C)
Location

Chromosome 9:121332522 (forward strand) | View in location tab

Co-located

with COSMIC COSM1459764 (T/C), COSM1459763 (T/C)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs3191330, rs1050966

This variant has 12 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

Variant displays