Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 5:132369935 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and is associated with 1 phenotype.

Variant displays