This variation has been flagged

Variation has more than 3 different alleles

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A/C/T | 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