Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
-/G
Location

Chromosome 18: between 51058149 and 51058150 (forward strand)|View in location tab

Most severe consequence
 
Frameshift variant
Evidence status

Clinical significance

Synonyms

LSDB SCV000042357, SCV000042358

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays