This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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


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

Most severe consequence
Evidence status

Clinical significance


Archive dbSNP rs3172624, rs60484582

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

Genotyping chips

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

About this variant

This variant overlaps 15 transcripts, has 1162 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays