Original source

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

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

About this variant

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

Variant displays