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rs878854341

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854341(C;GA)
Make rs878854341(GA;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17215294
GeneFLCN
is asnp
is mentioned by
dbSNPrs878854341
ebirs878854341
HLIrs878854341
Exacrs878854341
Varsomers878854341
Maprs878854341
PheGenIrs878854341
hapmaprs878854341
1000 genomesrs878854341
hgdprs878854341
ensemblrs878854341
gopubmedrs878854341
geneviewrs878854341
scholarrs878854341
googlers878854341
pharmgkbrs878854341
gwascentralrs878854341
openSNPrs878854341
23andMers878854341
23andMe allrs878854341
SNP Nexus

SNPshotrs878854341
SNPdbers878854341
MSV3drs878854341
GWAS Ctlgrs878854341
Max Magnitude0
ClinVar
Risk rs878854341(GA;GA)
Alt rs878854341(GA;GA)
Reference rs878854341(C;C)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17118608delGinsTC
CLNSRC
CLNACC RCV000003544.3,