Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.36 (G)
Location

Chromosome 13:33022051 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS043366

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs483961

HGVS names

This variant has 3 HGVS names - Hide

13:g.33022051A>G
ENST00000380099.3:c.819+4792A>G
ENST00000487852.1:n.827+4792A>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts, has 2776 sample genotypes and is mentioned in 3 citations.

Variant displays