rs876660611

Orientation

minus

Stabilized

minus

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

Make rs876660611(-;-)

Make rs876660611(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

17227949

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs876660611
dbSNP (classic)	rs876660611
ClinGen	rs876660611
ebi	rs876660611
HLI	rs876660611
Exac	rs876660611
Gnomad	rs876660611
Varsome	rs876660611
LitVar	rs876660611
Map	rs876660611
PheGenI	rs876660611
Biobank	rs876660611
1000 genomes	rs876660611
hgdp	rs876660611
ensembl	rs876660611
geneview	rs876660611
scholar	rs876660611
google	rs876660611
pharmgkb	rs876660611
gwascentral	rs876660611
openSNP	rs876660611
23andMe	rs876660611
SNPshot	rs876660611
SNPdbe	rs876660611
MSV3d	rs876660611
GWAS Ctlg	rs876660611

Max Magnitude

0

ClinVar
Risk	rs876660611(-;-)
Alt	rs876660611(-;-)
Reference	Rs876660611(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	FLCN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.17131263delG
CLNSRC
CLNACC	RCV000222065.1, RCV000255061.1,