Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.34 (G)
Location

Chromosome 16:3249749 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754869 (G/A), COSM3754868 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

Variation displays