rs755959303

Orientation

plus

Stabilized

plus

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

Make rs755959303(C;G)

Make rs755959303(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

17215184

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs755959303
dbSNP (classic)	rs755959303
ClinGen	rs755959303
ebi	rs755959303
HLI	rs755959303
Exac	rs755959303
Gnomad	rs755959303
Varsome	rs755959303
LitVar	rs755959303
Map	rs755959303
PheGenI	rs755959303
Biobank	rs755959303
1000 genomes	rs755959303
hgdp	rs755959303
ensembl	rs755959303
geneview	rs755959303
scholar	rs755959303
google	rs755959303
pharmgkb	rs755959303
gwascentral	rs755959303
openSNP	rs755959303
23andMe	rs755959303
SNPshot	rs755959303
SNPdbe	rs755959303
MSV3d	rs755959303
GWAS Ctlg	rs755959303

Max Magnitude

0

ClinVar
Risk	rs755959303(G;G) rs755959303(T;T)
Alt	rs755959303(G;G) rs755959303(T;T)
Reference	Rs755959303(C;C)
Significance	Pathogenic
Disease	Multiple fibrofolliculomas not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	FLCN LOC101928660
CLNDBN	Multiple fibrofolliculomas not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.17118498C>T
CLNSRC
CLNACC	RCV000239711.1, RCV000254996.3, RCV000492464.1,