Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:36592860 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB RAG2_1309G_A_010611

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts and is associated with 1 phenotype.

Variant displays