Original source

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

This variant has 2 HGVS names - click the plus to show

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

This variant has assays on 14 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2589 sample genotypes, is associated with 7 phenotypes and is mentioned in 24 citations.

Variant displays