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rs878855218

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855218(C;C)
Make rs878855218(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17221629
GeneFLCN
is asnp
is mentioned by
dbSNPrs878855218
ebirs878855218
HLIrs878855218
Exacrs878855218
Varsomers878855218
Maprs878855218
PheGenIrs878855218
hapmaprs878855218
1000 genomesrs878855218
hgdprs878855218
ensemblrs878855218
gopubmedrs878855218
geneviewrs878855218
scholarrs878855218
googlers878855218
pharmgkbrs878855218
gwascentralrs878855218
openSNPrs878855218
23andMers878855218
23andMe allrs878855218
SNP Nexus

SNPshotrs878855218
SNPdbers878855218
MSV3drs878855218
GWAS Ctlgrs878855218
Max Magnitude0
ClinVar
Risk rs878855218(C;C)
Alt rs878855218(C;C)
Reference rs878855218(G;G)
Significance Probable-Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17124943C>G
CLNSRC
CLNACC RCV000233680.1,