Have questions? Visit https://www.reddit.com/r/SNPedia

rs786203218

From SNPedia

Orientationminus
Geno Mag Summary
(TTC;TTC) 0 common in clinvar
Make rs786203218(-;-)
Make rs786203218(-;TTC)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position17224069
GeneFLCN
is asnp
is mentioned by
dbSNPrs786203218
ebirs786203218
HLIrs786203218
Exacrs786203218
Varsomers786203218
Maprs786203218
PheGenIrs786203218
hapmaprs786203218
1000 genomesrs786203218
hgdprs786203218
ensemblrs786203218
gopubmedrs786203218
geneviewrs786203218
scholarrs786203218
googlers786203218
pharmgkbrs786203218
gwascentralrs786203218
openSNPrs786203218
23andMers786203218
23andMe allrs786203218
SNP Nexus

SNPshotrs786203218
SNPdbers786203218
MSV3drs786203218
GWAS Ctlgrs786203218
Max Magnitude0
ClinVar
Risk rs786203218(;)
Alt rs786203218(;)
Reference rs786203218(TTC;TTC)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas
Variation info
Gene FLCN
CLNDBN Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas
Reversed 1
HGVS NC_000017.10:g.17127383_17127385delGAA
CLNSRC
CLNACC RCV000166434.1, RCV000239623.1,