Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 1:47417035 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062745

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_076_FOXE3_601094_0002, 9881

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

Variation displays