Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.48 (A)
Location

Chromosome 11:71308366 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs1792204, rs59491796

HGVS name

11:g.71308366G>A

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant has 6178 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays