Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 5:1279913 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 6 transcripts, has 2528 sample genotypes, is associated with 1 phenotype and is mentioned in 14 citations.

Variant displays