This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: 0.34 (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_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 22 transcripts and has 9 individual genotypes.

Variation displays