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
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.01 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

HGVS name

None

This variation has assays on 5 chips - click the plus to show

Variation displays