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 12:32843203 (forward strand) | View in location tab

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.10:g.32887404G>A

This variant has 9 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts and is associated with 1 phenotype.

Variant displays