Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.38 (A)
Location

Chromosome 16:56962376 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Hide

16:g.56962376G>A
ENST00000200676.7:c.118+279G>A
ENST00000566128.1:c.-78+80G>A
ENST00000569082.1:n.116+279G>A
ENST00000379780.6:c.118+279G>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2582 sample genotypes, is associated with 1 phenotype and is mentioned in 84 citations.

Variant displays