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rs1060502368

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502368(-;-)
Make rs1060502368(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17219060
GeneFLCN
is asnp
is mentioned by
dbSNPrs1060502368
dbSNP (old)rs1060502368
ClinGenrs1060502368
ebirs1060502368
HLIrs1060502368
Exacrs1060502368
Gnomadrs1060502368
Varsomers1060502368
Maprs1060502368
PheGenIrs1060502368
Biobankrs1060502368
1000 genomesrs1060502368
hgdprs1060502368
ensemblrs1060502368
gopubmedrs1060502368
geneviewrs1060502368
scholarrs1060502368
googlers1060502368
pharmgkbrs1060502368
gwascentralrs1060502368
openSNPrs1060502368
23andMers1060502368
23andMe allrs1060502368
SNPshotrs1060502368
SNPdbers1060502368
MSV3drs1060502368
GWAS Ctlgrs1060502368
Max Magnitude0
ClinVar
Risk rs1060502368(-;-)
Alt rs1060502368(-;-)
Reference Rs1060502368(C;C)
Significance Pathogenic
Disease Multiple fibrofolliculomas not provided Hereditary cancer-predisposing syndrome
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.17122374delG
CLNSRC
CLNACC RCV000470306.1, RCV000485342.1, RCV000492409.1,