Original source

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

Synonyms

Archive dbSNP rs1008239, rs60985891, rs861938

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2508 sample genotypes.

Variant displays