Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 8:89980833 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Broad13929737

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays