Original source

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

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5161

This variation has 17 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays