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rs398124523

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124523(C;T)
Make rs398124523(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17219021
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124523
ebirs398124523
HLIrs398124523
Exacrs398124523
Varsomers398124523
Maprs398124523
PheGenIrs398124523
hapmaprs398124523
1000 genomesrs398124523
hgdprs398124523
ensemblrs398124523
gopubmedrs398124523
geneviewrs398124523
scholarrs398124523
googlers398124523
pharmgkbrs398124523
gwascentralrs398124523
openSNPrs398124523
23andMers398124523
23andMe allrs398124523
SNP Nexus

SNPshotrs398124523
SNPdbers398124523
MSV3drs398124523
GWAS Ctlgrs398124523
Max Magnitude0
ClinVar
Risk rs398124523(T;T)
Alt rs398124523(T;T)
Reference rs398124523(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17122335G>A
CLNSRC ClinVar Emory University
CLNACC RCV000082617.4,