Have questions? Visit https://www.reddit.com/r/SNPedia

rs369869993

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs369869993(C;C)
Make rs369869993(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position70206159
GeneFADD
is asnp
is mentioned by
dbSNPrs369869993
ebirs369869993
HLIrs369869993
Exacrs369869993
Varsomers369869993
Maprs369869993
PheGenIrs369869993
hapmaprs369869993
1000 genomesrs369869993
hgdprs369869993
ensemblrs369869993
gopubmedrs369869993
geneviewrs369869993
scholarrs369869993
googlers369869993
pharmgkbrs369869993
gwascentralrs369869993
openSNPrs369869993
23andMers369869993
23andMe allrs369869993
SNP Nexus

SNPshotrs369869993
SNPdbers369869993
MSV3drs369869993
GWAS Ctlgrs369869993
Max Magnitude0
ClinVar
Risk rs369869993(C;C)
Alt rs369869993(C;C)
Reference rs369869993(T;T)
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.70052265T>C
CLNSRC
CLNACC RCV000195419.1,