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rs1060502367

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502367(A;A)
Make rs1060502367(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17221570
GeneFLCN
is asnp
is mentioned by
dbSNPrs1060502367
dbSNP (old)rs1060502367
ClinGenrs1060502367
ebirs1060502367
HLIrs1060502367
Exacrs1060502367
Gnomadrs1060502367
Varsomers1060502367
Maprs1060502367
PheGenIrs1060502367
Biobankrs1060502367
1000 genomesrs1060502367
hgdprs1060502367
ensemblrs1060502367
gopubmedrs1060502367
geneviewrs1060502367
scholarrs1060502367
googlers1060502367
pharmgkbrs1060502367
gwascentralrs1060502367
openSNPrs1060502367
23andMers1060502367
23andMe allrs1060502367
SNPshotrs1060502367
SNPdbers1060502367
MSV3drs1060502367
GWAS Ctlgrs1060502367
Max Magnitude0
ClinVar
Risk rs1060502367(A;A)
Alt rs1060502367(A;A)
Reference Rs1060502367(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17124884C>A; NC_000017.10:g.17124884C>T
CLNSRC
CLNACC RCV000492583.1, RCV000463825.1,