Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 11:36593483 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_278_RAG2_179616_0002, 5156

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 44 transcripts and is associated with 3 phenotypes.

Variant displays