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rs398124539

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124539(-;-)
Make rs398124539(-;TG)
Make rs398124539(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome17
Position17221578
GeneFLCN
is asnp
is mentioned by
dbSNPrs398124539
ebirs398124539
HLIrs398124539
Exacrs398124539
Varsomers398124539
Maprs398124539
PheGenIrs398124539
hapmaprs398124539
1000 genomesrs398124539
hgdprs398124539
ensemblrs398124539
gopubmedrs398124539
geneviewrs398124539
scholarrs398124539
googlers398124539
pharmgkbrs398124539
gwascentralrs398124539
openSNPrs398124539
23andMers398124539
23andMe allrs398124539
SNP Nexus

SNPshotrs398124539
SNPdbers398124539
MSV3drs398124539
GWAS Ctlgrs398124539
Max Magnitude0
ClinVar
Risk rs398124539(TG;TG)
Alt rs398124539(TG;TG)
Reference rs398124539(;)
Significance Pathogenic
Disease not provided
Variation info
Gene FLCN
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.17124893_17124894dupCA
CLNSRC ClinVar
CLNACC RCV000082642.3,