Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 12:52287296 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT81:c.1053T>C (G/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs11170085, rs11552018

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

Variation displays