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rs786205468

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205468(C;C)
Make rs786205468(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position36593622
GeneC11orf74, RAG2
is asnp
is mentioned by
dbSNPrs786205468
ebirs786205468
HLIrs786205468
Exacrs786205468
Varsomers786205468
Maprs786205468
PheGenIrs786205468
hapmaprs786205468
1000 genomesrs786205468
hgdprs786205468
ensemblrs786205468
gopubmedrs786205468
geneviewrs786205468
scholarrs786205468
googlers786205468
pharmgkbrs786205468
gwascentralrs786205468
openSNPrs786205468
23andMers786205468
23andMe allrs786205468
SNP Nexus

SNPshotrs786205468
SNPdbers786205468
MSV3drs786205468
GWAS Ctlgrs786205468
Max Magnitude0
ClinVar
Risk rs786205468(C;C)
Alt rs786205468(C;C)
Reference rs786205468(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG2 C11orf74
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.36615172A>G
CLNSRC
CLNACC RCV000171193.1,