Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.02 (C)
Location

Chromosome 22:29277932 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs17454586

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2576 sample genotypes.

Variant displays