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rs878855221

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855221(-;-)
Make rs878855221(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17219094
GeneFLCN
is asnp
is mentioned by
dbSNPrs878855221
ebirs878855221
HLIrs878855221
Exacrs878855221
Varsomers878855221
Maprs878855221
PheGenIrs878855221
hapmaprs878855221
1000 genomesrs878855221
hgdprs878855221
ensemblrs878855221
gopubmedrs878855221
geneviewrs878855221
scholarrs878855221
googlers878855221
pharmgkbrs878855221
gwascentralrs878855221
openSNPrs878855221
23andMers878855221
23andMe allrs878855221
SNP Nexus

SNPshotrs878855221
SNPdbers878855221
MSV3drs878855221
GWAS Ctlgrs878855221
Max Magnitude0
ClinVar
Risk rs878855221(;)
Alt rs878855221(;)
Reference rs878855221(C;C)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17122408delG
CLNSRC
CLNACC RCV000226049.1,