Original source

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

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

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

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Clinical significance

Synonyms

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