Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.34 (G)
Location

Chromosome 13:33049027 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS043365

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Hide

13:g.33049027G>A
ENST00000380099.3:c.820-4740G>A
ENST00000487852.1:n.828-4740G>A

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts, has 2776 sample genotypes and is mentioned in 2 citations.

Variant displays