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rs758385503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758385503(-;-)
Make rs758385503(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position17228089
GeneFLCN
is asnp
is mentioned by
dbSNPrs758385503
dbSNP (classic)rs758385503
ClinGenrs758385503
ebirs758385503
HLIrs758385503
Exacrs758385503
Gnomadrs758385503
Varsomers758385503
LitVarrs758385503
Maprs758385503
PheGenIrs758385503
Biobankrs758385503
1000 genomesrs758385503
hgdprs758385503
ensemblrs758385503
geneviewrs758385503
scholarrs758385503
googlers758385503
pharmgkbrs758385503
gwascentralrs758385503
openSNPrs758385503
23andMers758385503
SNPshotrs758385503
SNPdbers758385503
MSV3drs758385503
GWAS Ctlgrs758385503
Max Magnitude0
ClinVar
Risk rs758385503(-;-)
Alt rs758385503(-;-)
Reference Rs758385503(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.17131403delG
CLNSRC
CLNACC RCV000485925.1,