Original source

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

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

Chromosome 9:136508238 (forward strand) | View in location tab


with HGMD-PUBLIC CM053346

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 5810

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts, has 2 sample genotypes and is associated with 2 phenotypes.

Variant displays