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rs755959303

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs755959303(C;G)
Make rs755959303(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position17215184
GeneFLCN
is asnp
is mentioned by
dbSNPrs755959303
ebirs755959303
HLIrs755959303
Exacrs755959303
Varsomers755959303
Maprs755959303
PheGenIrs755959303
hapmaprs755959303
1000 genomesrs755959303
hgdprs755959303
ensemblrs755959303
gopubmedrs755959303
geneviewrs755959303
scholarrs755959303
googlers755959303
pharmgkbrs755959303
gwascentralrs755959303
openSNPrs755959303
23andMers755959303
23andMe allrs755959303
SNP Nexus

SNPshotrs755959303
SNPdbers755959303
MSV3drs755959303
GWAS Ctlgrs755959303
Max Magnitude0
ClinVar
Risk rs755959303(G;G)
Alt rs755959303(G;G)
Reference rs755959303(C;C)
Significance Pathogenic
Disease Multiple fibrofolliculomas
Variation info
Gene FLCN LOC101928660
CLNDBN Multiple fibrofolliculomas
Reversed 0
HGVS NC_000017.10:g.17118498C>T
CLNSRC
CLNACC RCV000239711.1,