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

rs398124527

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124527(-;-)
Make rs398124527(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position17215312
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124527
ebirs398124527
HLIrs398124527
Exacrs398124527
Varsomers398124527
Maprs398124527
PheGenIrs398124527
hapmaprs398124527
1000 genomesrs398124527
hgdprs398124527
ensemblrs398124527
gopubmedrs398124527
geneviewrs398124527
scholarrs398124527
googlers398124527
pharmgkbrs398124527
gwascentralrs398124527
openSNPrs398124527
23andMers398124527
23andMe allrs398124527
SNP Nexus

SNPshotrs398124527
SNPdbers398124527
MSV3drs398124527
GWAS Ctlgrs398124527
Max Magnitude0
ClinVar
Risk rs398124527(;)
Alt rs398124527(;)
Reference rs398124527(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN LOC101928660
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17118626delA
CLNSRC HGMD
CLNACC RCV000082627.4,