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rs786205469

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs786205469(-;-)
Make rs786205469(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position36593794
GeneC11orf74, RAG2
is asnp
is mentioned by
dbSNPrs786205469
ebirs786205469
HLIrs786205469
Exacrs786205469
Varsomers786205469
Maprs786205469
PheGenIrs786205469
hapmaprs786205469
1000 genomesrs786205469
hgdprs786205469
ensemblrs786205469
gopubmedrs786205469
geneviewrs786205469
scholarrs786205469
googlers786205469
pharmgkbrs786205469
gwascentralrs786205469
openSNPrs786205469
23andMers786205469
23andMe allrs786205469
SNP Nexus

SNPshotrs786205469
SNPdbers786205469
MSV3drs786205469
GWAS Ctlgrs786205469
Max Magnitude0
ClinVar
Risk rs786205469(;)
Alt rs786205469(;)
Reference rs786205469(CA;CA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG2 C11orf74
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.36615344_36615345delTG
CLNSRC
CLNACC RCV000171194.1,