Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.30 (C)

Chromosome 22:50582239 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 25 transcripts, 1 regulatory feature, has 2511 sample genotypes and is associated with 1 phenotype.

Variant displays