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 9:136677537 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3905808 ; HGMD-PUBLIC CM020918

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_007_AGPAT2_603100_0001, 11640

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and is associated with 2 phenotypes.

Variant displays