rs398124528

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs398124528(A;G)

Make rs398124528(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17215092

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124528
dbSNP (classic)	rs398124528
ClinGen	rs398124528
ebi	rs398124528
HLI	rs398124528
Exac	rs398124528
Gnomad	rs398124528
Varsome	rs398124528
LitVar	rs398124528
Map	rs398124528
PheGenI	rs398124528
Biobank	rs398124528
1000 genomes	rs398124528
hgdp	rs398124528
ensembl	rs398124528
geneview	rs398124528
scholar	rs398124528
google	rs398124528
pharmgkb	rs398124528
gwascentral	rs398124528
openSNP	rs398124528
23andMe	rs398124528
SNPshot	rs398124528
SNPdbe	rs398124528
MSV3d	rs398124528
GWAS Ctlg	rs398124528

Max Magnitude

0

ClinVar
Risk	rs398124528(G;G)
Alt	rs398124528(G;G)
Reference	Rs398124528(A;A)
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.17118406T>C
CLNSRC	ClinVar
CLNACC	RCV000082628.5, RCV000166694.1,