Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.08 (A)
Location

Chromosome 11:89277878 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17800907, rs56750720

HGVS names

This variant has 2 HGVS names - Hide

11:g.89277878G>A
ENST00000263321.5:c.1185-6895G>A

Genotyping chips

This variant has assays on 14 chips - Show

About this variant

This variant overlaps 1 transcript, has 3821 sample genotypes, is associated with 7 phenotypes and is mentioned in 25 citations.

Variant displays