Original source

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

This variant has 3 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

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

Variant displays