Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (C)
Location

Chromosome 5:112845224 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2507 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays