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rs1064793251

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position36593630
GeneC11orf74, RAG2
is asnp
is mentioned by
dbSNPrs1064793251
dbSNP (old)rs1064793251
ClinGenrs1064793251
ebirs1064793251
HLIrs1064793251
Exacrs1064793251
Gnomadrs1064793251
Varsomers1064793251
Maprs1064793251
PheGenIrs1064793251
Biobankrs1064793251
1000 genomesrs1064793251
hgdprs1064793251
ensemblrs1064793251
gopubmedrs1064793251
geneviewrs1064793251
scholarrs1064793251
googlers1064793251
pharmgkbrs1064793251
gwascentralrs1064793251
openSNPrs1064793251
23andMers1064793251
23andMe allrs1064793251
SNPshotrs1064793251
SNPdbers1064793251
MSV3drs1064793251
GWAS Ctlgrs1064793251
Max Magnitude0
ClinVar
Risk rs1064793251(A;A)
Alt rs1064793251(A;A)
Reference Rs1064793251(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RAG2 C11orf74
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.36615180G>T
CLNSRC
CLNACC RCV000481067.1,