Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 16:23621451 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NM_024675.3:c.3024C>T

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays