Have questions? Visit https://www.reddit.com/r/SNPedia

rs398124526

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124526(-;-)
Make rs398124526(-;C)
Make rs398124526(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position17216476
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124526
ebirs398124526
HLIrs398124526
Exacrs398124526
Varsomers398124526
Maprs398124526
PheGenIrs398124526
hapmaprs398124526
1000 genomesrs398124526
hgdprs398124526
ensemblrs398124526
gopubmedrs398124526
geneviewrs398124526
scholarrs398124526
googlers398124526
pharmgkbrs398124526
gwascentralrs398124526
openSNPrs398124526
23andMers398124526
23andMe allrs398124526
SNP Nexus

SNPshotrs398124526
SNPdbers398124526
MSV3drs398124526
GWAS Ctlgrs398124526
Max Magnitude0
ClinVar
Risk rs398124526(C;C)
Alt rs398124526(C;C)
Reference rs398124526(;)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN LOC101928660
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17119791dupG
CLNSRC ClinVar
CLNACC RCV000082623.3,