Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 12:13717508 (forward strand) | View in location tab

Co-located

with COSMIC COSM430806 (G/A) ; HGMD-PUBLIC CM074898

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 2 HGVS names - click the plus to show

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

Variation displays