This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/C | Ambiguity code: M
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

LSDB NG_029922.1:g.9498G>T

HGVS name

None

Variation displays