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rs876658390

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658390(-;-)
Make rs876658390(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17228079
GeneFLCN
is asnp
is mentioned by
dbSNPrs876658390
ebirs876658390
HLIrs876658390
Exacrs876658390
Varsomers876658390
Maprs876658390
PheGenIrs876658390
hapmaprs876658390
1000 genomesrs876658390
hgdprs876658390
ensemblrs876658390
gopubmedrs876658390
geneviewrs876658390
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googlers876658390
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openSNPrs876658390
23andMers876658390
23andMe allrs876658390
SNP Nexus

SNPshotrs876658390
SNPdbers876658390
MSV3drs876658390
GWAS Ctlgrs876658390
Max Magnitude0
ClinVar
Risk rs876658390(;)
Alt rs876658390(;)
Reference rs876658390(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17131393delA
CLNSRC
CLNACC RCV000213153.1, RCV000239668.1,