Original source

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

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

Chromosome 1:226888945 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM034894

Most severe consequence
Evidence status

Clinical significance

Synonyms

PhenCode ADM_227

This variation has 11 HGVS names - click the plus to show

Variation displays