Original source

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

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

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

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB RAG2_1309G_A_010611

HGVS names

This variant has 10 HGVS names - Show

About this variant

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

Variant displays