Original source

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

Alleles
A/G/T|Ancestral: A|Ambiguity code: D|MAF: 0.24 (A)
Location

Chromosome 11:71435645 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

HGVS names

This variant has 26 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 16 transcripts, has 3912 sample genotypes and is associated with 1 phenotype.

Variant displays