Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 11:36576246 (forward strand) | View in location tab


with HGMD-PUBLIC CM054093 ; PhenCode RAG1base_RAG1_DNA:g.9234A>C (A/C)

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

Variation displays