Have questions? Visit https://www.reddit.com/r/SNPedia

rs35691292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35691292(C;T)
Make rs35691292(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position36593525
GeneC11orf74, RAG2
is asnp
is mentioned by
dbSNPrs35691292
ebirs35691292
HLIrs35691292
Exacrs35691292
Varsomers35691292
Maprs35691292
PheGenIrs35691292
hapmaprs35691292
1000 genomesrs35691292
hgdprs35691292
ensemblrs35691292
gopubmedrs35691292
geneviewrs35691292
scholarrs35691292
googlers35691292
pharmgkbrs35691292
gwascentralrs35691292
openSNPrs35691292
23andMers35691292
23andMe allrs35691292
SNP Nexus

SNPshotrs35691292
SNPdbers35691292
MSV3drs35691292
GWAS Ctlgrs35691292
Max Magnitude0
OMIM179616
Desc
Variant0007
Relatedalso
? (C;C) (C;T)
ClinVar
Risk rs35691292(A,T;A,T)
Alt rs35691292(A,T;A,T)
Reference rs35691292(C;C)
Significance Pathogenic
Disease Severe combined immunodeficiency
Variation info
Gene RAG2 C11orf74
CLNDBN Severe combined immunodeficiency, b cell-negative
Reversed 1
HGVS NC_000011.9:g.36615075G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014016.24,