Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.29 (T)

Chromosome 1:145927267 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

Clinical significance


LSDB NG_032654.1:g.5270A>T

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 31 transcripts, 1 regulatory feature, has 3240 sample genotypes and is associated with 1 phenotype.

Variant displays