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rs748486078

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748486078(A;A)
Make rs748486078(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position52237139
GeneIL17F, LOC105375088
is asnp
is mentioned by
dbSNPrs748486078
ebirs748486078
HLIrs748486078
Exacrs748486078
Varsomers748486078
Maprs748486078
PheGenIrs748486078
hapmaprs748486078
1000 genomesrs748486078
hgdprs748486078
ensemblrs748486078
gopubmedrs748486078
geneviewrs748486078
scholarrs748486078
googlers748486078
pharmgkbrs748486078
gwascentralrs748486078
openSNPrs748486078
23andMers748486078
23andMe allrs748486078
SNP Nexus

SNPshotrs748486078
SNPdbers748486078
MSV3drs748486078
GWAS Ctlgrs748486078
Max Magnitude0
ClinVar
Risk rs748486078(A;A)
Alt rs748486078(A;A)
Reference rs748486078(G;G)
Significance Pathogenic
Disease Candidiasis
Variation info
Gene IL17F
CLNDBN Candidiasis, familial, 6
Reversed 0
HGVS NC_000006.11:g.52101937G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023553.3,