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rs398122364

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122364(C;T)
Make rs398122364(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136371345
GeneCARD9
is asnp
is mentioned by
dbSNPrs398122364
ebirs398122364
HLIrs398122364
Exacrs398122364
Varsomers398122364
Maprs398122364
PheGenIrs398122364
hapmaprs398122364
1000 genomesrs398122364
hgdprs398122364
ensemblrs398122364
gopubmedrs398122364
geneviewrs398122364
scholarrs398122364
googlers398122364
pharmgkbrs398122364
gwascentralrs398122364
openSNPrs398122364
23andMers398122364
23andMe allrs398122364
SNP Nexus

SNPshotrs398122364
SNPdbers398122364
MSV3drs398122364
GWAS Ctlgrs398122364
Max Magnitude0
ClinVar
Risk rs398122364(T;T)
Alt rs398122364(T;T)
Reference rs398122364(C;C)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene CARD9 DNLZ
CLNDBN Candidiasis, familial, 2
Reversed 1
HGVS NC_000009.11:g.139265797G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074441.3,