Original source

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

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

Chromosome 11:6391976 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM920624

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 15098

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 27 transcripts and is associated with 4 phenotypes.

Variant displays