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rs398124528

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398124528(A;G)
Make rs398124528(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position17215092
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124528
ebirs398124528
HLIrs398124528
Exacrs398124528
Varsomers398124528
Maprs398124528
PheGenIrs398124528
hapmaprs398124528
1000 genomesrs398124528
hgdprs398124528
ensemblrs398124528
gopubmedrs398124528
geneviewrs398124528
scholarrs398124528
googlers398124528
pharmgkbrs398124528
gwascentralrs398124528
openSNPrs398124528
23andMers398124528
23andMe allrs398124528
SNP Nexus

SNPshotrs398124528
SNPdbers398124528
MSV3drs398124528
GWAS Ctlgrs398124528
Max Magnitude0
ClinVar
Risk rs398124528(G;G)
Alt rs398124528(G;G)
Reference rs398124528(A;A)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene FLCN LOC101928660
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.17118406T>C
CLNSRC ClinVar
CLNACC RCV000082628.4, RCV000166694.1,