Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.35 (A)
Location

Chromosome 16:23629146 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3696 sample genotypes, is associated with 2 phenotypes and is mentioned in 6 citations.

Variant displays