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rs398124529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs398124529(-;-)
Make rs398124529(-;AAG)
ReferenceGRCh38 38.1/141
Chromosome17
Position17214999
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124529
ebirs398124529
HLIrs398124529
Exacrs398124529
Varsomers398124529
Maprs398124529
PheGenIrs398124529
hapmaprs398124529
1000 genomesrs398124529
hgdprs398124529
ensemblrs398124529
gopubmedrs398124529
geneviewrs398124529
scholarrs398124529
googlers398124529
pharmgkbrs398124529
gwascentralrs398124529
openSNPrs398124529
23andMers398124529
23andMe allrs398124529
SNP Nexus

SNPshotrs398124529
SNPdbers398124529
MSV3drs398124529
GWAS Ctlgrs398124529
Max Magnitude0
ClinVar
Risk rs398124529(;)
Alt rs398124529(;)
Reference rs398124529(AAG;AAG)
Significance Pathogenic
Disease not provided Multiple fibrofolliculomas
Variation info
Gene FLCN LOC101928660
CLNDBN not provided Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17118313_17118315delCTT
CLNSRC HGMD
CLNACC RCV000082629.4, RCV000239713.1,