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rs863225091

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225091(C;T)
Make rs863225091(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151813569
GeneRORC
is asnp
is mentioned by
dbSNPrs863225091
ebirs863225091
HLIrs863225091
Exacrs863225091
Varsomers863225091
Maprs863225091
PheGenIrs863225091
hapmaprs863225091
1000 genomesrs863225091
hgdprs863225091
ensemblrs863225091
gopubmedrs863225091
geneviewrs863225091
scholarrs863225091
googlers863225091
pharmgkbrs863225091
gwascentralrs863225091
openSNPrs863225091
23andMers863225091
23andMe allrs863225091
SNP Nexus

SNPshotrs863225091
SNPdbers863225091
MSV3drs863225091
GWAS Ctlgrs863225091
Max Magnitude0
ClinVar
Risk rs863225091(T;T)
Alt rs863225091(T;T)
Reference rs863225091(C;C)
Significance Pathogenic
Disease Immunodeficiency 42
Variation info
Gene RORC
CLNDBN Immunodeficiency 42
Reversed 1
HGVS NC_000001.10:g.151786045G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201359.2,