Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:36597174 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961216 ; PhenCode RAG1base_HSRAG1:g.2432G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5133, 2010_April_001_265_RAG1_179615_0002

This variation has 9 HGVS names - click the plus to show

Variation displays