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rs786202541

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202541(C;G)
Make rs786202541(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position17216465
GeneFLCN
is asnp
is mentioned by
dbSNPrs786202541
ebirs786202541
HLIrs786202541
Exacrs786202541
Varsomers786202541
Maprs786202541
PheGenIrs786202541
hapmaprs786202541
1000 genomesrs786202541
hgdprs786202541
ensemblrs786202541
gopubmedrs786202541
geneviewrs786202541
scholarrs786202541
googlers786202541
pharmgkbrs786202541
gwascentralrs786202541
openSNPrs786202541
23andMers786202541
23andMe allrs786202541
SNP Nexus

SNPshotrs786202541
SNPdbers786202541
MSV3drs786202541
GWAS Ctlgrs786202541
Max Magnitude0
ClinVar
Risk rs786202541(G;G)
Alt rs786202541(G;G)
Reference rs786202541(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FLCN LOC101928660
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.17119779G>C
CLNSRC
CLNACC RCV000165394.1,