Original source

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

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

Chromosome 11:2884750 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM970250

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 9590, 2010_April_001_027_CDKN1C_600856_0004

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is associated with 2 phenotypes.

Variant displays