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
A/C/G/T | Ancestral: A | Ambiguity code: N | MAF: 0.40 (G)
Location

Chromosome 13:27666691 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 4229 individual genotypes.

Variation displays