Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 HGVS names - click the plus to show

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

This variant has assays on 5 chips - click the plus to 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 79 citations.

Variant displays