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rs878855220

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878855220(AGA;AGA)
Make rs878855220(AGA;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17221580
GeneFLCN
is asnp
is mentioned by
dbSNPrs878855220
ebirs878855220
HLIrs878855220
Exacrs878855220
Varsomers878855220
Maprs878855220
PheGenIrs878855220
hapmaprs878855220
1000 genomesrs878855220
hgdprs878855220
ensemblrs878855220
gopubmedrs878855220
geneviewrs878855220
scholarrs878855220
googlers878855220
pharmgkbrs878855220
gwascentralrs878855220
openSNPrs878855220
23andMers878855220
23andMe allrs878855220
SNP Nexus

SNPshotrs878855220
SNPdbers878855220
MSV3drs878855220
GWAS Ctlgrs878855220
Max Magnitude0
ClinVar
Risk rs878855220(AGA;AGA)
Alt rs878855220(AGA;AGA)
Reference rs878855220(T;T)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17124894delAinsTCT
CLNSRC
CLNACC RCV000231805.1,