Original source

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

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

Chromosome 11:36592817 (forward strand) | View in location tab


with HGMD-PUBLIC CM081770 ; PhenCode RAG2base_RAG2_DNA:g.6420G>C (C/G)

Most severe consequence
Evidence status

Clinical significance


LSDB 5164

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

About this variant

This variant overlaps 22 transcripts and is associated with 2 phenotypes.

Variation displays