Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 11:44581778 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3762 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays