Original source

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

A/G/T | Ancestral: A | Ambiguity code: D | MAF: 0.18 (A)

Chromosome 11:71435645 (forward strand) | View in location tab


with COSMIC COSM429787 (A/G), COSM1475860 (A/G)

Most severe consequence
Evidence status

Clinical significance

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

This variation has assays on 7 chips - click the plus to show

Variation displays