This variant maps to 6 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

This variant maps to 6 genomic locations; None selected

Synonyms

LSDB NG_029922.1:g.9497T>G, NG_029922.1:g.9497T>A

HGVS name

None

Variant displays