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rs137852930

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852930(C;G)
Make rs137852930(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position17227902
GeneFLCN
is asnp
is mentioned by
dbSNPrs137852930
ebirs137852930
HLIrs137852930
Exacrs137852930
Varsomers137852930
Maprs137852930
PheGenIrs137852930
hapmaprs137852930
1000 genomesrs137852930
hgdprs137852930
ensemblrs137852930
gopubmedrs137852930
geneviewrs137852930
scholarrs137852930
googlers137852930
pharmgkbrs137852930
gwascentralrs137852930
openSNPrs137852930
23andMers137852930
23andMe allrs137852930
SNP Nexus

SNPshotrs137852930
SNPdbers137852930
MSV3drs137852930
GWAS Ctlgrs137852930
Max Magnitude0
OMIM607273
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852930(G;G)
Alt rs137852930(G;G)
Reference rs137852930(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene FLCN
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000017.10:g.17131216G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003536.4,