This variation maps to 7 locations

Select a location:
Original source

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

Alleles
C/A/T | Ambiguity code: H
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms

LSDB NG_029922.1:g.11284G>A, NG_029922.1:g.11284G>T

HGVS name

None

Variation displays