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rs398124540

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124540(-;-)
Make rs398124540(-;C)
Make rs398124540(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position17228054
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124540
ebirs398124540
HLIrs398124540
Exacrs398124540
Varsomers398124540
Maprs398124540
PheGenIrs398124540
hapmaprs398124540
1000 genomesrs398124540
hgdprs398124540
ensemblrs398124540
gopubmedrs398124540
geneviewrs398124540
scholarrs398124540
googlers398124540
pharmgkbrs398124540
gwascentralrs398124540
openSNPrs398124540
23andMers398124540
23andMe allrs398124540
SNP Nexus

SNPshotrs398124540
SNPdbers398124540
MSV3drs398124540
GWAS Ctlgrs398124540
Max Magnitude0
ClinVar
Risk rs398124540(C;C)
Alt rs398124540(C;C)
Reference rs398124540(;)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17131369dupG
CLNSRC ClinVar
CLNACC RCV000082643.3,