rs398124525

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;C)	5	Birt-Hogg-Dube Syndrome
(C;C)	0	common in clinvar

Make rs398124525(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17216501

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124525
dbSNP (classic)	rs398124525
ClinGen	rs398124525
ebi	rs398124525
HLI	rs398124525
Exac	rs398124525
Gnomad	rs398124525
Varsome	rs398124525
LitVar	rs398124525
Map	rs398124525
PheGenI	rs398124525
Biobank	rs398124525
1000 genomes	rs398124525
hgdp	rs398124525
ensembl	rs398124525
geneview	rs398124525
scholar	rs398124525
google	rs398124525
pharmgkb	rs398124525
gwascentral	rs398124525
openSNP	rs398124525
23andMe	rs398124525
SNPshot	rs398124525
SNPdbe	rs398124525
MSV3d	rs398124525
GWAS Ctlg	rs398124525

Max Magnitude

5

ClinVar
Risk	rs398124525(-;-)
Alt	rs398124525(-;-)
Reference	Rs398124525(C;C)
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.17119815delG
CLNSRC	ClinVar
CLNACC	RCV000082621.5, RCV000492656.1,