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rs150739647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150739647(A;A)
Make rs150739647(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position36576228
GeneRAG1
is asnp
is mentioned by
dbSNPrs150739647
dbSNP (old)rs150739647
ClinGenrs150739647
ebirs150739647
HLIrs150739647
Exacrs150739647
Gnomadrs150739647
Varsomers150739647
Maprs150739647
PheGenIrs150739647
Biobankrs150739647
1000 genomesrs150739647
hgdprs150739647
ensemblrs150739647
gopubmedrs150739647
geneviewrs150739647
scholarrs150739647
googlers150739647
pharmgkbrs150739647
gwascentralrs150739647
openSNPrs150739647
23andMers150739647
23andMe allrs150739647
SNPshotrs150739647
SNPdbers150739647
MSV3drs150739647
GWAS Ctlgrs150739647
Max Magnitude0
ClinVar
Risk rs150739647(A;A) rs150739647(C;C)
Alt rs150739647(A;A) rs150739647(C;C)
Reference Rs150739647(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RAG1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.36597778G>A
CLNSRC UniProtKB (protein) UniProtKB (variants)
CLNACC RCV000059574.2,