Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.14 (A)
Location

Chromosome 12:52302264 (forward strand) | View in location tab

Co-located

with COSMIC COSM4147201 (G/A) ; PhenCode HIFD_KRT86:c.348G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

Variation displays