Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.33 (C)
Location

Chromosome 5:112828541 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, has 2511 sample genotypes and is associated with 1 phenotype.

Variant displays