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rs398122362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122362(A;A)
Make rs398122362(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position136371432
GeneCARD9
is asnp
is mentioned by
dbSNPrs398122362
ebirs398122362
HLIrs398122362
Exacrs398122362
Varsomers398122362
Maprs398122362
PheGenIrs398122362
hapmaprs398122362
1000 genomesrs398122362
hgdprs398122362
ensemblrs398122362
gopubmedrs398122362
geneviewrs398122362
scholarrs398122362
googlers398122362
pharmgkbrs398122362
gwascentralrs398122362
openSNPrs398122362
23andMers398122362
23andMe allrs398122362
SNP Nexus

SNPshotrs398122362
SNPdbers398122362
MSV3drs398122362
GWAS Ctlgrs398122362
Max Magnitude0
ClinVar
Risk rs398122362(A;A)
Alt rs398122362(A;A)
Reference rs398122362(G;G)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene CARD9 DNLZ
CLNDBN Candidiasis, familial, 2
Reversed 1
HGVS NC_000009.11:g.139265884C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074438.3,