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rs786205616

From SNPedia

Orientationminus
Geno Mag Summary
(ATCT;ATCT) 0 common in clinvar
Make rs786205616(-;-)
Make rs786205616(-;ATCT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position36592763
GeneC11orf74, RAG2
is asnp
is mentioned by
dbSNPrs786205616
ebirs786205616
HLIrs786205616
Exacrs786205616
Varsomers786205616
Maprs786205616
PheGenIrs786205616
hapmaprs786205616
1000 genomesrs786205616
hgdprs786205616
ensemblrs786205616
gopubmedrs786205616
geneviewrs786205616
scholarrs786205616
googlers786205616
pharmgkbrs786205616
gwascentralrs786205616
openSNPrs786205616
23andMers786205616
23andMe allrs786205616
SNP Nexus

SNPshotrs786205616
SNPdbers786205616
MSV3drs786205616
GWAS Ctlgrs786205616
Max Magnitude0
ClinVar
Risk rs786205616(;)
Alt rs786205616(;)
Reference rs786205616(ATCT;ATCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG2 C11orf74
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.36614313_36614316delAGAT
CLNSRC
CLNACC RCV000171462.1,