rs786202081

Orientation

minus

Stabilized

minus

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

Make rs786202081(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

17226323

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs786202081
dbSNP (classic)	rs786202081
ClinGen	rs786202081
ebi	rs786202081
HLI	rs786202081
Exac	rs786202081
Gnomad	rs786202081
Varsome	rs786202081
LitVar	rs786202081
Map	rs786202081
PheGenI	rs786202081
Biobank	rs786202081
1000 genomes	rs786202081
hgdp	rs786202081
ensembl	rs786202081
geneview	rs786202081
scholar	rs786202081
google	rs786202081
pharmgkb	rs786202081
gwascentral	rs786202081
openSNP	rs786202081
23andMe	rs786202081
SNPshot	rs786202081
SNPdbe	rs786202081
MSV3d	rs786202081
GWAS Ctlg	rs786202081

Max Magnitude

5

ClinVar
Risk	rs786202081(A;A)
Alt	rs786202081(A;A)
Reference	Rs786202081(G;G)
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.17129637C>T
CLNSRC
CLNACC	RCV000164717.2, RCV000239714.1, RCV000490144.1,