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rs1060502369

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502369(G;T)
Make rs1060502369(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17227888
GeneFLCN
is asnp
is mentioned by
dbSNPrs1060502369
dbSNP (old)rs1060502369
ClinGenrs1060502369
ebirs1060502369
HLIrs1060502369
Exacrs1060502369
Gnomadrs1060502369
Varsomers1060502369
Maprs1060502369
PheGenIrs1060502369
Biobankrs1060502369
1000 genomesrs1060502369
hgdprs1060502369
ensemblrs1060502369
gopubmedrs1060502369
geneviewrs1060502369
scholarrs1060502369
googlers1060502369
pharmgkbrs1060502369
gwascentralrs1060502369
openSNPrs1060502369
23andMers1060502369
23andMe allrs1060502369
SNPshotrs1060502369
SNPdbers1060502369
MSV3drs1060502369
GWAS Ctlgrs1060502369
Max Magnitude0
ClinVar
Risk rs1060502369(T;T)
Alt rs1060502369(T;T)
Reference Rs1060502369(G;G)
Significance Probable-Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17131202C>A
CLNSRC
CLNACC RCV000473630.1,