This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: G | Ambiguity code: N | MAF: 0.22 (A)
Location

Chromosome 4:6302360 (forward strand) | View in location tab

Co-located

with COSMIC COSM448013 (A/G) ; HGMD-PUBLIC CM021366

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3172624, rs60484582

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

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo, Illumina_HumanOmni2.5

About this variant

This variant overlaps 15 transcripts, has 2560 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays