Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 2:46607420 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080232, CM081583

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11790, 11789

This variation has 8 HGVS names - click the plus to show

Variation displays