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
T/G/A/C | Ancestral: T | Ambiguity code: N | MAF: 0.32 (G)
Location

Chromosome 14:22552027 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays