Original source

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

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

Chromosome 12:52696048 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

Variation displays