Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.47 (G)
Location

Chromosome 16:89792600 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs74251563, rs17232546

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2600 sample genotypes.

Variant displays