Original source

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

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

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

Co-located

with HGMD-PUBLIC CM053346

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 5810

This variant has 3 HGVS names - click the plus to 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