Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)

Chromosome 8:89935181 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

Clinical significance


LSDB Broad13929681

HGVS names

This variant has 7 HGVS names - Show

About this variant

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

Variant displays