Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.47 (C)
Location

Chromosome 9:286593 (forward strand) | View in location tab

Co-located

with COSMIC COSM3763874 (C/A), COSM3763875 (C/A)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 22 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

Variation displays