Original source

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

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

Chromosome 11:36594065 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001326 ; PhenCode RAG2base_HSRAG2X:g.1305G>T (C/A), RAG2base_RAG2_DNA:g.5172G>T (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB RAG2_104G_C_010611

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

Variation displays