Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 18:31592983 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910374, CM962553, CM840006

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4875, 4837

This variation has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is associated with 4 phenotypes.

Variation displays