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 (T)
Location

Chromosome 13:27623299 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR115454

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 11 transcripts, has 4255 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays