Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.03 (A)
Location

Chromosome 16:30751910 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs57330689

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2511 sample genotypes.

Variant displays