This variation has been flagged

  • None of the variant alleles match the reference allele
  • Variation has more than 3 different alleles
Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.11 (A)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 8 synonyms - click the plus to show

HGVS name

None

This variation has assays on 4 chips - click the plus to show

Variation displays