Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.31 (G)
Location

Chromosome 22:22630997 (forward strand) | View in location tab

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

This variation has 5 synonyms - click the plus to show

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2543 individual genotypes.

Variation displays