Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.39 (A)
Location

Chromosome 12:52676361 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT1:c.1389C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

Variation displays