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rs878854340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTTACAGAGTT;GTTACAGAGTT) 0 common in clinvar
Make rs878854340(-;-)
Make rs878854340(-;GTTACAGAGTT)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17215313
GeneFLCN
is asnp
is mentioned by
dbSNPrs878854340
dbSNP (classic)rs878854340
ClinGenrs878854340
ebirs878854340
HLIrs878854340
Exacrs878854340
Gnomadrs878854340
Varsomers878854340
LitVarrs878854340
Maprs878854340
PheGenIrs878854340
Biobankrs878854340
1000 genomesrs878854340
hgdprs878854340
ensemblrs878854340
geneviewrs878854340
scholarrs878854340
googlers878854340
pharmgkbrs878854340
gwascentralrs878854340
openSNPrs878854340
23andMers878854340
SNPshotrs878854340
SNPdbers878854340
MSV3drs878854340
GWAS Ctlgrs878854340
Max Magnitude0
ClinVar
Risk rs878854340(-;-)
Alt rs878854340(-;-)
Reference Rs878854340(GTTACAGAGTT;GTTACAGAGTT)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN LOC101928660
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17118627_17118637delAACTCTGTAAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000003544.3,