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rs878855213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878855213(-;-)
Make rs878855213(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17216461
GeneFLCN
is asnp
is mentioned by
dbSNPrs878855213
dbSNP (old)rs878855213
ClinGenrs878855213
ebirs878855213
HLIrs878855213
Exacrs878855213
Gnomadrs878855213
Varsomers878855213
Maprs878855213
PheGenIrs878855213
Biobankrs878855213
1000 genomesrs878855213
hgdprs878855213
ensemblrs878855213
gopubmedrs878855213
geneviewrs878855213
scholarrs878855213
googlers878855213
pharmgkbrs878855213
gwascentralrs878855213
openSNPrs878855213
23andMers878855213
23andMe allrs878855213
SNP Nexus

SNPshotrs878855213
SNPdbers878855213
MSV3drs878855213
GWAS Ctlgrs878855213
Max Magnitude0
ClinVar
Risk rs878855213(-;-)
Alt rs878855213(-;-)
Reference Rs878855213(A;A)
Significance Pathogenic
Disease Multiple fibrofolliculomas not provided
Variation info
Gene FLCN LOC101928660
CLNDBN Multiple fibrofolliculomas not provided
Reversed 1
HGVS NC_000017.10:g.17119775delT
CLNSRC
CLNACC RCV000228856.1, RCV000255255.2,