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rs878855212

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855212(-;-)
Make rs878855212(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17228025
GeneFLCN
is asnp
is mentioned by
dbSNPrs878855212
ebirs878855212
HLIrs878855212
Exacrs878855212
Varsomers878855212
Maprs878855212
PheGenIrs878855212
hapmaprs878855212
1000 genomesrs878855212
hgdprs878855212
ensemblrs878855212
gopubmedrs878855212
geneviewrs878855212
scholarrs878855212
googlers878855212
pharmgkbrs878855212
gwascentralrs878855212
openSNPrs878855212
23andMers878855212
23andMe allrs878855212
SNP Nexus

SNPshotrs878855212
SNPdbers878855212
MSV3drs878855212
GWAS Ctlgrs878855212
Max Magnitude0
ClinVar
Risk rs878855212(;)
Alt rs878855212(;)
Reference rs878855212(G;G)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17131339delC
CLNSRC
CLNACC RCV000233508.1,