rs398124527

Orientation

minus

Stabilized

minus

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

Make rs398124527(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17215312

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124527
dbSNP (classic)	rs398124527
ClinGen	rs398124527
ebi	rs398124527
HLI	rs398124527
Exac	rs398124527
Gnomad	rs398124527
Varsome	rs398124527
LitVar	rs398124527
Map	rs398124527
PheGenI	rs398124527
Biobank	rs398124527
1000 genomes	rs398124527
hgdp	rs398124527
ensembl	rs398124527
geneview	rs398124527
scholar	rs398124527
google	rs398124527
pharmgkb	rs398124527
gwascentral	rs398124527
openSNP	rs398124527
23andMe	rs398124527
SNPshot	rs398124527
SNPdbe	rs398124527
MSV3d	rs398124527
GWAS Ctlg	rs398124527

Max Magnitude

5

ClinVar
Risk	rs398124527(-;-)
Alt	rs398124527(-;-)
Reference	Rs398124527(T;T)
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.17118626delA
CLNSRC	HGMD
CLNACC	RCV000082627.4, RCV000492221.1,