Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NG_032654.1:g.5270A>T

This variation has 22 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 27 transcripts, has 3240 individual genotypes and is associated with 1 phenotype.

Variation displays