Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:36594046 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981698 ; PhenCode RAG2base_HSRAG2X:g.1324C>G (G/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5157, 2010_April_001_279_RAG2_179616_0003

This variation has 13 HGVS names - click the plus to show

Variation displays