This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
A/C/G/T | Ancestral: G | Ambiguity code: N | MAF: 0.21 (G)
Location

Chromosome 19:41263403 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 45 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays