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rs398124535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs398124535(CAC;CAC)
Make rs398124535(CAC;GT)
ReferenceGRCh38 38.1/141
Chromosome17
Position17226252
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124535
ebirs398124535
HLIrs398124535
Exacrs398124535
Varsomers398124535
Maprs398124535
PheGenIrs398124535
hapmaprs398124535
1000 genomesrs398124535
hgdprs398124535
ensemblrs398124535
gopubmedrs398124535
geneviewrs398124535
scholarrs398124535
googlers398124535
pharmgkbrs398124535
gwascentralrs398124535
openSNPrs398124535
23andMers398124535
23andMe allrs398124535
SNP Nexus

SNPshotrs398124535
SNPdbers398124535
MSV3drs398124535
GWAS Ctlgrs398124535
Max Magnitude0
ClinVar
Risk rs398124535(CAC;CAC)
Alt rs398124535(CAC;CAC)
Reference rs398124535(GT;GT)
Significance Pathogenic
Disease not provided Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN not provided Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17129566_17129567delACinsGTG
CLNSRC HGMD
CLNACC RCV000082635.4, RCV000239674.1,