Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.34 (C)
Location

Chromosome 22:29289722 (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 rs1008239, rs60985891, rs861938

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

About this variant

This variant overlaps 16 transcripts and has 2508 individual genotypes.

Variation displays