Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 5 HGVS names - Hide

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

Genotyping chips

This variant has assays on 10 chips - 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 26 citations.

Variant displays