Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 12:52700021 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990785, CM993348 ; PhenCode HIFD_KRT86:c.1204G>A (G/A), HIFD_KRT86:c.1204G>C (G/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variation displays