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rs876658409

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658409(A;A)
Make rs876658409(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17223983
GeneFLCN
is asnp
is mentioned by
dbSNPrs876658409
ebirs876658409
HLIrs876658409
Exacrs876658409
Varsomers876658409
Maprs876658409
PheGenIrs876658409
hapmaprs876658409
1000 genomesrs876658409
hgdprs876658409
ensemblrs876658409
gopubmedrs876658409
geneviewrs876658409
scholarrs876658409
googlers876658409
pharmgkbrs876658409
gwascentralrs876658409
openSNPrs876658409
23andMers876658409
23andMe allrs876658409
SNP Nexus

SNPshotrs876658409
SNPdbers876658409
MSV3drs876658409
GWAS Ctlgrs876658409
Max Magnitude0
ClinVar
Risk rs876658409(A;A)
Alt rs876658409(A;A)
Reference rs876658409(G;G)
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.17127297C>T
CLNSRC
CLNACC RCV000217378.1,