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 11:6394204 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041858, CM910355

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 15089

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts and is associated with 3 phenotypes.

Variant displays