This variation maps to 2 locations

Select a location:
Original source

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

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

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 9590, 2010_April_001_027_CDKN1C_600856_0004

HGVS name

None

About this variant

This variant is associated with 3 phenotypes.

Variation displays