Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:36597018 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961215 ; PhenCode RAG1base_HSRAG1:g.2276G>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

Variation displays