Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:2905980 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970250

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9590, 2010_April_001_027_CDKN1C_600856_0004

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

Variation displays