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rs387906839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906839(G;G)
Make rs387906839(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position70206161
GeneFADD
is asnp
is mentioned by
dbSNPrs387906839
ebirs387906839
HLIrs387906839
Exacrs387906839
Varsomers387906839
Maprs387906839
PheGenIrs387906839
hapmaprs387906839
1000 genomesrs387906839
hgdprs387906839
ensemblrs387906839
gopubmedrs387906839
geneviewrs387906839
scholarrs387906839
googlers387906839
pharmgkbrs387906839
gwascentralrs387906839
openSNPrs387906839
23andMers387906839
23andMe allrs387906839
SNP Nexus

SNPshotrs387906839
SNPdbers387906839
MSV3drs387906839
GWAS Ctlgrs387906839
Max Magnitude0
ClinVar
Risk rs387906839(G;G)
Alt rs387906839(G;G)
Reference rs387906839(T;T)
Significance Pathogenic
Disease Infections
Variation info
Gene FADD
CLNDBN Infections, recurrent, associated with encephalopathy, hepatic dysfunction, and cardiovascular malformations
Reversed 0
HGVS NC_000011.9:g.70052267T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023196.2,