rs876658390

Orientation

minus

Stabilized

minus

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

Make rs876658390(-;-)

Make rs876658390(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

17228079

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs876658390
dbSNP (classic)	rs876658390
ClinGen	rs876658390
ebi	rs876658390
HLI	rs876658390
Exac	rs876658390
Gnomad	rs876658390
Varsome	rs876658390
LitVar	rs876658390
Map	rs876658390
PheGenI	rs876658390
Biobank	rs876658390
1000 genomes	rs876658390
hgdp	rs876658390
ensembl	rs876658390
geneview	rs876658390
scholar	rs876658390
google	rs876658390
pharmgkb	rs876658390
gwascentral	rs876658390
openSNP	rs876658390
23andMe	rs876658390
SNPshot	rs876658390
SNPdbe	rs876658390
MSV3d	rs876658390
GWAS Ctlg	rs876658390

Max Magnitude

0

ClinVar
Risk	rs876658390(-;-)
Alt	rs876658390(-;-)
Reference	Rs876658390(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas not provided
Variation	info
Gene	FLCN
CLNDBN	Hereditary cancer-predisposing syndrome Multiple fibrofolliculomas not provided
Reversed	1
HGVS	NC_000017.10:g.17131393delA
CLNSRC
CLNACC	RCV000213153.1, RCV000239668.1, RCV000256007.2,