Original source

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

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2578 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays