Original source

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

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

Chromosome 18:31595152 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910376, CM890113

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4854, 4838

This variation has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and is associated with 4 phenotypes.

Variation displays