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rs1060502371

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060502371(-;-)
Make rs1060502371(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17227899
GeneFLCN
is asnp
is mentioned by
dbSNPrs1060502371
dbSNP (old)rs1060502371
ClinGenrs1060502371
ebirs1060502371
HLIrs1060502371
Exacrs1060502371
Gnomadrs1060502371
Varsomers1060502371
Maprs1060502371
PheGenIrs1060502371
Biobankrs1060502371
1000 genomesrs1060502371
hgdprs1060502371
ensemblrs1060502371
gopubmedrs1060502371
geneviewrs1060502371
scholarrs1060502371
googlers1060502371
pharmgkbrs1060502371
gwascentralrs1060502371
openSNPrs1060502371
23andMers1060502371
23andMe allrs1060502371
SNPshotrs1060502371
SNPdbers1060502371
MSV3drs1060502371
GWAS Ctlgrs1060502371
Max Magnitude0
ClinVar
Risk rs1060502371(-;-)
Alt rs1060502371(-;-)
Reference Rs1060502371(A;A)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17131213delT
CLNSRC
CLNACC RCV000461846.1,