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
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

This variation has 5 synonyms - click the plus to show

HGVS name

None

This variation has assays on 6 chips - click the plus to show

Variation displays