This variation maps to 2 locations

Select a location:
Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

This variation maps to 2 genomic locations; None selected

Clinical significance

Synonyms

LSDB 33485, 33484

HGVS name

None

Variation displays