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rs137852929

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852929(C;G)
Make rs137852929(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position17215228
GeneFLCN
is asnp
is mentioned by
dbSNPrs137852929
ebirs137852929
HLIrs137852929
Exacrs137852929
Varsomers137852929
Maprs137852929
PheGenIrs137852929
hapmaprs137852929
1000 genomesrs137852929
hgdprs137852929
ensemblrs137852929
gopubmedrs137852929
geneviewrs137852929
scholarrs137852929
googlers137852929
pharmgkbrs137852929
gwascentralrs137852929
openSNPrs137852929
23andMers137852929
23andMe allrs137852929
SNP Nexus

SNPshotrs137852929
SNPdbers137852929
MSV3drs137852929
GWAS Ctlgrs137852929
Max Magnitude0
OMIM607273
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137852929(G,T;G,T)
Alt rs137852929(G,T;G,T)
Reference rs137852929(C;C)
Significance Pathogenic
Disease Multiple fibrofolliculomas Hereditary cancer-predisposing syndrome
Variation info
Gene FLCN LOC101928660
CLNDBN Multiple fibrofolliculomas Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.17118542G>A; NC_000017.10:g.17118542G>C; NC_000017.10:g.17118542G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000225850.1, RCV000003534.3, RCV000166580.1, RCV000239639.1,