Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 13:33054107 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB NM_004795.3:c.1160G>A

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

Variant displays