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rs398124525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124525(-;-)
Make rs398124525(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position17216501
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124525
ClinGenrs398124525
ebirs398124525
HLIrs398124525
Exacrs398124525
Varsomers398124525
Maprs398124525
PheGenIrs398124525
hapmaprs398124525
1000 genomesrs398124525
hgdprs398124525
ensemblrs398124525
gopubmedrs398124525
geneviewrs398124525
scholarrs398124525
googlers398124525
pharmgkbrs398124525
gwascentralrs398124525
openSNPrs398124525
23andMers398124525
23andMe allrs398124525
SNP Nexus

SNPshotrs398124525
SNPdbers398124525
MSV3drs398124525
GWAS Ctlgrs398124525
Max Magnitude0
ClinVar
Risk rs398124525(-;-)
Alt rs398124525(-;-)
Reference Rs398124525(C;C)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene FLCN LOC101928660
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.17119815delG
CLNSRC ClinVar
CLNACC RCV000082621.5, RCV000492656.1,