Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: < 0.01 (A)
Location

Chromosome 8:89971047 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Broad13929728

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays