rs398124526

Orientation

minus

Stabilized

minus

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

Make rs398124526(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17216476

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124526
dbSNP (classic)	rs398124526
ClinGen	rs398124526
ebi	rs398124526
HLI	rs398124526
Exac	rs398124526
Gnomad	rs398124526
Varsome	rs398124526
LitVar	rs398124526
Map	rs398124526
PheGenI	rs398124526
Biobank	rs398124526
1000 genomes	rs398124526
hgdp	rs398124526
ensembl	rs398124526
geneview	rs398124526
scholar	rs398124526
google	rs398124526
pharmgkb	rs398124526
gwascentral	rs398124526
openSNP	rs398124526
23andMe	rs398124526
SNPshot	rs398124526
SNPdbe	rs398124526
MSV3d	rs398124526
GWAS Ctlg	rs398124526

Max Magnitude

5

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	RCV000082623.4,