rs1060502368

Orientation

minus

Stabilized

minus

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

Make rs1060502368(-;-)

Make rs1060502368(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

17219060

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs1060502368
dbSNP (classic)	rs1060502368
ClinGen	rs1060502368
ebi	rs1060502368
HLI	rs1060502368
Exac	rs1060502368
Gnomad	rs1060502368
Varsome	rs1060502368
LitVar	rs1060502368
Map	rs1060502368
PheGenI	rs1060502368
Biobank	rs1060502368
1000 genomes	rs1060502368
hgdp	rs1060502368
ensembl	rs1060502368
geneview	rs1060502368
scholar	rs1060502368
google	rs1060502368
pharmgkb	rs1060502368
gwascentral	rs1060502368
openSNP	rs1060502368
23andMe	rs1060502368
SNPshot	rs1060502368
SNPdbe	rs1060502368
MSV3d	rs1060502368
GWAS Ctlg	rs1060502368

Max Magnitude

0

ClinVar
Risk	rs1060502368(-;-)
Alt	rs1060502368(-;-)
Reference	Rs1060502368(C;C)
Significance	Pathogenic
Disease	Multiple fibrofolliculomas not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	FLCN
CLNDBN	Multiple fibrofolliculomas not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.17122374delG
CLNSRC
CLNACC	RCV000470306.1, RCV000485342.1, RCV000492409.1,