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rs786205615

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205615(-;-)
Make rs786205615(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position36573858
GeneRAG1
is asnp
is mentioned by
dbSNPrs786205615
ebirs786205615
HLIrs786205615
Exacrs786205615
Varsomers786205615
Maprs786205615
PheGenIrs786205615
hapmaprs786205615
1000 genomesrs786205615
hgdprs786205615
ensemblrs786205615
gopubmedrs786205615
geneviewrs786205615
scholarrs786205615
googlers786205615
pharmgkbrs786205615
gwascentralrs786205615
openSNPrs786205615
23andMers786205615
23andMe allrs786205615
SNP Nexus

SNPshotrs786205615
SNPdbers786205615
MSV3drs786205615
GWAS Ctlgrs786205615
Max Magnitude0
ClinVar
Risk rs786205615(;)
Alt rs786205615(;)
Reference rs786205615(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.36595408delG
CLNSRC
CLNACC RCV000171461.1,