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rs863224871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGAGCAG;CGAGCAG) 0 common in clinvar
Make rs863224871(-;-)
Make rs863224871(-;AGCGAGC)
Make rs863224871(AGCGAGC;AGCGAGC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position70203511
GeneFADD
is asnp
is mentioned by
dbSNPrs863224871
dbSNP (old)rs863224871
ClinGenrs863224871
ebirs863224871
HLIrs863224871
Exacrs863224871
Gnomadrs863224871
Varsomers863224871
Maprs863224871
PheGenIrs863224871
Biobankrs863224871
1000 genomesrs863224871
hgdprs863224871
ensemblrs863224871
gopubmedrs863224871
geneviewrs863224871
scholarrs863224871
googlers863224871
pharmgkbrs863224871
gwascentralrs863224871
openSNPrs863224871
23andMers863224871
23andMe allrs863224871
SNP Nexus

SNPshotrs863224871
SNPdbers863224871
MSV3drs863224871
GWAS Ctlgrs863224871
Max Magnitude0
ClinVar
Risk rs863224871(-;-)
Alt rs863224871(-;-)
Reference Rs863224871(CGAGCAG;CGAGCAG)
Significance Probable-Pathogenic
Disease Infections
Variation info
Gene FADD
CLNDBN Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
Reversed 0
HGVS NC_000011.9:g.70049617_70049623delAGCGAGC
CLNSRC
CLNACC RCV000195419.1,