Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:67490059 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM104862

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.490C>T

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature and is associated with 1 phenotype.

Variant displays