Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 11:36593525 (forward strand) | View in location tab


with PhenCode RAG2base_RAG2_DNA:g.5712C>T (G/A)

Most severe consequence
Evidence status

Clinical significance


LSDB 5161

This variation has 18 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 44 transcripts, has 128 individual genotypes and is associated with 2 phenotypes.

Variation displays