Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H
Location

Chromosome 18:29172946 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM840006, CM910374, CM962553

Most severe consequence
Clinical significance

Synonyms

LSDB 4837, 4875

This variation has 10 HGVS names - click the plus to show

Variation displays