This variant maps to 3 locations

Select a location:
Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs34395043

HGVS name

None

Variant displays