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rs587777075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777075(A;A)
Make rs587777075(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position1213738
GeneTNFRSF4
is asnp
is mentioned by
dbSNPrs587777075
ebirs587777075
HLIrs587777075
Exacrs587777075
Varsomers587777075
Maprs587777075
PheGenIrs587777075
hapmaprs587777075
1000 genomesrs587777075
hgdprs587777075
ensemblrs587777075
gopubmedrs587777075
geneviewrs587777075
scholarrs587777075
googlers587777075
pharmgkbrs587777075
gwascentralrs587777075
openSNPrs587777075
23andMers587777075
23andMe allrs587777075
SNP Nexus

SNPshotrs587777075
SNPdbers587777075
MSV3drs587777075
GWAS Ctlgrs587777075
Max Magnitude0
ClinVar
Risk rs587777075(A;A)
Alt rs587777075(A;A)
Reference rs587777075(G;G)
Significance Pathogenic
Disease IMMUNODEFICIENCY 16 (1 patient)
Variation info
Gene TNFRSF4
CLNDBN IMMUNODEFICIENCY 16 (1 patient)
Reversed 0
HGVS NC_000001.10:g.1149118G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000082860.5,