This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N | MAF: 0.41 (G)
Location

Chromosome 13:27666691 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 12 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays