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rs863225092

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225092(C;T)
Make rs863225092(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position151811399
GeneRORC
is asnp
is mentioned by
dbSNPrs863225092
ebirs863225092
HLIrs863225092
Exacrs863225092
Varsomers863225092
Maprs863225092
PheGenIrs863225092
hapmaprs863225092
1000 genomesrs863225092
hgdprs863225092
ensemblrs863225092
gopubmedrs863225092
geneviewrs863225092
scholarrs863225092
googlers863225092
pharmgkbrs863225092
gwascentralrs863225092
openSNPrs863225092
23andMers863225092
23andMe allrs863225092
SNP Nexus

SNPshotrs863225092
SNPdbers863225092
MSV3drs863225092
GWAS Ctlgrs863225092
Max Magnitude0
ClinVar
Risk rs863225092(T;T)
Alt rs863225092(T;T)
Reference rs863225092(C;C)
Significance Pathogenic
Disease Immunodeficiency 42
Variation info
Gene RORC
CLNDBN Immunodeficiency 42
Reversed 1
HGVS NC_000001.10:g.151783875G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201397.2,