Original source

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

This variant has assays on 13 chips - click the plus to show

About this variant

This variant has 4537 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays