Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)

Chromosome 22:50525476 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

Clinical significance


ClinVar SCV000171601

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 30 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays