Original source

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

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

Chromosome 16:89768689 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17233092, rs58404229

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2594 sample genotypes.

Variant displays