Original source

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

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

Chromosome 11:36597668 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961218 ; PhenCode RAG1base_HSRAG1:g.2926T>G (T/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5134, 2010_April_001_266_RAG1_179615_0003

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

Variation displays