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rs398124532

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124532(C;T)
Make rs398124532(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17213798
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124532
ebirs398124532
HLIrs398124532
Exacrs398124532
Varsomers398124532
Maprs398124532
PheGenIrs398124532
hapmaprs398124532
1000 genomesrs398124532
hgdprs398124532
ensemblrs398124532
gopubmedrs398124532
geneviewrs398124532
scholarrs398124532
googlers398124532
pharmgkbrs398124532
gwascentralrs398124532
openSNPrs398124532
23andMers398124532
23andMe allrs398124532
SNP Nexus

SNPshotrs398124532
SNPdbers398124532
MSV3drs398124532
GWAS Ctlgrs398124532
Max Magnitude0
ClinVar
Risk rs398124532(T;T)
Alt rs398124532(T;T)
Reference rs398124532(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN LOC101928660
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17117112G>A
CLNSRC HGMD
CLNACC RCV000082632.4,