Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:67487155 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS104882

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.249G>T

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and is associated with 1 phenotype.

Variant displays