This variation has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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

Variation displays