Original source

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

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

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


with 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