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: 0.21 (G)

Chromosome 19:40757498 (forward strand) | View in location tab


with COSMIC COSM4000739 (A/G)

Most severe consequence
Evidence status

This variation has 45 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_Human1M-duo

About this variant

This variant overlaps 30 transcripts and has 2647 individual genotypes.

Variation displays