Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:36574986 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981694 ; PhenCode RAG1base_HSRAG1:g.1794G>A (G/A), RAG1base_RAG1_DNA:g.7974G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays