Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
Evidence status

Synonyms

This variant has 6 synonyms - Show

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2543 sample genotypes.

Variant displays