Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.31 (A)
Location

Chromosome 16:56971567 (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.56971567C>A
ENST00000200676.7:c.658+186C>A
ENST00000566128.1:c.463+186C>A
ENST00000569082.1:n.760+186C>A
ENST00000379780.6:c.658+186C>A

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 3963 sample genotypes, is associated with 9 phenotypes and is mentioned in 25 citations.

Variant displays