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
T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: 0.36 (T)
Location

Chromosome 7:93540348 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays