Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.12 (C)
Location

Chromosome 22:50581640 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs5770787

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts, has 2773 individual genotypes and is mentioned in 1 citation.

Variation displays