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rs149712114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149712114(C;T)
Make rs149712114(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136367788
GeneCARD9
is asnp
is mentioned by
dbSNPrs149712114
ebirs149712114
HLIrs149712114
Exacrs149712114
Varsomers149712114
Maprs149712114
PheGenIrs149712114
hapmaprs149712114
1000 genomesrs149712114
hgdprs149712114
ensemblrs149712114
gopubmedrs149712114
geneviewrs149712114
scholarrs149712114
googlers149712114
pharmgkbrs149712114
gwascentralrs149712114
openSNPrs149712114
23andMers149712114
23andMe allrs149712114
SNP Nexus

SNPshotrs149712114
SNPdbers149712114
MSV3drs149712114
GWAS Ctlgrs149712114
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs149712114(G,T;G,T)
Alt rs149712114(G,T;G,T)
Reference rs149712114(C;C)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene CARD9 DNLZ
CLNDBN Candidiasis, familial, 2
Reversed 0
HGVS NC_000009.11:g.139262240C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000074439.5,