Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.22 (A)
Location

Chromosome 6:32589658 (forward strand) | View in location tab

Co-located

with COSMIC COSM4160979 (A/C)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays