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rs387906913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906913(C;T)
Make rs387906913(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position17104729
GeneIL17RA
is asnp
is mentioned by
dbSNPrs387906913
dbSNP (classic)rs387906913
ClinGenrs387906913
ebirs387906913
HLIrs387906913
Exacrs387906913
Gnomadrs387906913
Varsomers387906913
LitVarrs387906913
Maprs387906913
PheGenIrs387906913
Biobankrs387906913
1000 genomesrs387906913
hgdprs387906913
ensemblrs387906913
geneviewrs387906913
scholarrs387906913
googlers387906913
pharmgkbrs387906913
gwascentralrs387906913
openSNPrs387906913
23andMers387906913
SNPshotrs387906913
SNPdbers387906913
MSV3drs387906913
GWAS Ctlgrs387906913
Max Magnitude0
ClinVar
Risk rs387906913(T;T)
Alt rs387906913(T;T)
Reference Rs387906913(C;C)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene IL17RA
CLNDBN Candidiasis, familial, 5
Reversed 0
HGVS NC_000022.10:g.17585619C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023443.4,