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rs786202081

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202081(A;A)
Make rs786202081(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position17226323
GeneFLCN
is asnp
is mentioned by
dbSNPrs786202081
ebirs786202081
HLIrs786202081
Exacrs786202081
Varsomers786202081
Maprs786202081
PheGenIrs786202081
hapmaprs786202081
1000 genomesrs786202081
hgdprs786202081
ensemblrs786202081
gopubmedrs786202081
geneviewrs786202081
scholarrs786202081
googlers786202081
pharmgkbrs786202081
gwascentralrs786202081
openSNPrs786202081
23andMers786202081
23andMe allrs786202081
SNP Nexus

SNPshotrs786202081
SNPdbers786202081
MSV3drs786202081
GWAS Ctlgrs786202081
Max Magnitude0
ClinVar
Risk rs786202081(A;A)
Alt rs786202081(A;A)
Reference rs786202081(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.17129637C>T
CLNSRC
CLNACC RCV000164717.1, RCV000239714.1,