This variation 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 (mapped to GRCh38) (release 138) | View in dbSNP

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

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

HGVS name

None

Variation displays