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: 0.20 (C)
Location

Chromosome 13:27921083 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs4616145, rs116914624

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 6 transcripts and has 2506 individual genotypes.

Variation displays