Original source

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

Alleles
A/C | Ambiguity code: M | MAF: 0.32 (C)
Location

Chromosome 3:184380405 (forward strand) | View in location tab

Co-located

with COSMIC COSM4157476 (A/C), COSM4157477 (A/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74286221

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

Variation displays