Original source

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

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

Chromosome 11:71146691 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

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