Original source

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

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts.

Variant displays