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rs149229197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149229197(G;T)
Make rs149229197(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position36573831
GeneRAG1
is asnp
is mentioned by
dbSNPrs149229197
dbSNP (old)rs149229197
ClinGenrs149229197
ebirs149229197
HLIrs149229197
Exacrs149229197
Gnomadrs149229197
Varsomers149229197
Maprs149229197
PheGenIrs149229197
Biobankrs149229197
1000 genomesrs149229197
hgdprs149229197
ensemblrs149229197
gopubmedrs149229197
geneviewrs149229197
scholarrs149229197
googlers149229197
pharmgkbrs149229197
gwascentralrs149229197
openSNPrs149229197
23andMers149229197
23andMe allrs149229197
SNPshotrs149229197
SNPdbers149229197
MSV3drs149229197
GWAS Ctlgrs149229197
Max Magnitude0
ClinVar
Risk rs149229197(T;T)
Alt rs149229197(T;T)
Reference Rs149229197(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.36595381G>T
CLNSRC
CLNACC RCV000413643.1,