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rs199474690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199474690(A;T)
Make rs199474690(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position36575868
GeneRAG1
is asnp
is mentioned by
dbSNPrs199474690
dbSNP (old)rs199474690
ClinGenrs199474690
ebirs199474690
HLIrs199474690
Exacrs199474690
Gnomadrs199474690
Varsomers199474690
Maprs199474690
PheGenIrs199474690
Biobankrs199474690
1000 genomesrs199474690
hgdprs199474690
ensemblrs199474690
gopubmedrs199474690
geneviewrs199474690
scholarrs199474690
googlers199474690
pharmgkbrs199474690
gwascentralrs199474690
openSNPrs199474690
23andMers199474690
23andMe allrs199474690
SNPshotrs199474690
SNPdbers199474690
MSV3drs199474690
GWAS Ctlgrs199474690
Max Magnitude0
ClinVar
Risk rs199474690(G;G) rs199474690(T;T)
Alt rs199474690(G;G) rs199474690(T;T)
Reference Rs199474690(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.36597418A>G; NC_000011.9:g.36597418A>T
CLNSRC UniProtKB (protein) UniProtKB (variants)
CLNACC RCV000480355.1, RCV000059572.1,