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rs878855217

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855217(-;-)
Make rs878855217(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17223956
GeneFLCN
is asnp
is mentioned by
dbSNPrs878855217
ebirs878855217
HLIrs878855217
Exacrs878855217
Varsomers878855217
Maprs878855217
PheGenIrs878855217
hapmaprs878855217
1000 genomesrs878855217
hgdprs878855217
ensemblrs878855217
gopubmedrs878855217
geneviewrs878855217
scholarrs878855217
googlers878855217
pharmgkbrs878855217
gwascentralrs878855217
openSNPrs878855217
23andMers878855217
23andMe allrs878855217
SNP Nexus

SNPshotrs878855217
SNPdbers878855217
MSV3drs878855217
GWAS Ctlgrs878855217
Max Magnitude0
ClinVar
Risk rs878855217(;)
Alt rs878855217(;)
Reference rs878855217(G;G)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17127270delC
CLNSRC
CLNACC RCV000230881.2,