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rs121918338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918338(C;T)
Make rs121918338(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136370362
GeneCARD9
is asnp
is mentioned by
dbSNPrs121918338
ebirs121918338
HLIrs121918338
Exacrs121918338
Varsomers121918338
Maprs121918338
PheGenIrs121918338
hapmaprs121918338
1000 genomesrs121918338
hgdprs121918338
ensemblrs121918338
gopubmedrs121918338
geneviewrs121918338
scholarrs121918338
googlers121918338
pharmgkbrs121918338
gwascentralrs121918338
openSNPrs121918338
23andMers121918338
23andMe allrs121918338
SNP Nexus

SNPshotrs121918338
SNPdbers121918338
MSV3drs121918338
GWAS Ctlgrs121918338
Max Magnitude0
OMIM607212
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918338(T;T)
Alt rs121918338(T;T)
Reference rs121918338(C;C)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene CARD9 DNLZ
CLNDBN Candidiasis, familial, 2
Reversed 1
HGVS NC_000009.11:g.139264814G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003575.2,