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rs398122363

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122363(C;T)
Make rs398122363(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136370380
GeneCARD9
is asnp
is mentioned by
dbSNPrs398122363
ebirs398122363
HLIrs398122363
Exacrs398122363
Varsomers398122363
Maprs398122363
PheGenIrs398122363
hapmaprs398122363
1000 genomesrs398122363
hgdprs398122363
ensemblrs398122363
gopubmedrs398122363
geneviewrs398122363
scholarrs398122363
googlers398122363
pharmgkbrs398122363
gwascentralrs398122363
openSNPrs398122363
23andMers398122363
23andMe allrs398122363
SNP Nexus

SNPshotrs398122363
SNPdbers398122363
MSV3drs398122363
GWAS Ctlgrs398122363
Max Magnitude0
ClinVar
Risk rs398122363(T;T)
Alt rs398122363(T;T)
Reference rs398122363(C;C)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene CARD9 DNLZ
CLNDBN Candidiasis, familial, 2
Reversed 1
HGVS NC_000009.11:g.139264832G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074440.4,