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rs876660611

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660611(-;-)
Make rs876660611(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17227949
GeneFLCN
is asnp
is mentioned by
dbSNPrs876660611
ebirs876660611
HLIrs876660611
Exacrs876660611
Varsomers876660611
Maprs876660611
PheGenIrs876660611
hapmaprs876660611
1000 genomesrs876660611
hgdprs876660611
ensemblrs876660611
gopubmedrs876660611
geneviewrs876660611
scholarrs876660611
googlers876660611
pharmgkbrs876660611
gwascentralrs876660611
openSNPrs876660611
23andMers876660611
23andMe allrs876660611
SNP Nexus

SNPshotrs876660611
SNPdbers876660611
MSV3drs876660611
GWAS Ctlgrs876660611
Max Magnitude0
ClinVar
Risk rs876660611(;)
Alt rs876660611(;)
Reference rs876660611(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FLCN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.17131263delG
CLNSRC
CLNACC RCV000222065.1,