This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs34569076

HGVS name

None

Variant displays