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 26 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 32 transcripts, 1 regulatory feature, has 3240 sample genotypes and is associated with 1 phenotype.

Variant displays