Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 14:73640295 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961199, CM981652

Most severe consequence
Evidence status

Clinical significance

Synonyms

PhenCode ADM_99, ADM_10

This variation has 28 HGVS names - click the plus to show

Variation displays