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
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.10 (T)
Location

Chromosome 14:77275628 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117725279, rs58133087

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays