Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (G)
Location

Chromosome 16:3304762 (forward strand) | View in location tab

Co-located

with COSMIC COSM435205 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 16 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays