Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 8:89978491 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


LSDB Broad13929735

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays