rs1060502369

Orientation

minus

Stabilized

minus

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

Make rs1060502369(G;T)

Make rs1060502369(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

17227888

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs1060502369
dbSNP (classic)	rs1060502369
ClinGen	rs1060502369
ebi	rs1060502369
HLI	rs1060502369
Exac	rs1060502369
Gnomad	rs1060502369
Varsome	rs1060502369
LitVar	rs1060502369
Map	rs1060502369
PheGenI	rs1060502369
Biobank	rs1060502369
1000 genomes	rs1060502369
hgdp	rs1060502369
ensembl	rs1060502369
geneview	rs1060502369
scholar	rs1060502369
google	rs1060502369
pharmgkb	rs1060502369
gwascentral	rs1060502369
openSNP	rs1060502369
23andMe	rs1060502369
SNPshot	rs1060502369
SNPdbe	rs1060502369
MSV3d	rs1060502369
GWAS Ctlg	rs1060502369

Max Magnitude

0

ClinVar
Risk	rs1060502369(T;T)
Alt	rs1060502369(T;T)
Reference	Rs1060502369(G;G)
Significance	Probable-Pathogenic
Disease	Multiple fibrofolliculomas
Variation	info
Gene	FLCN
CLNDBN	Multiple fibrofolliculomas
Reversed	1
HGVS	NC_000017.10:g.17131202C>A
CLNSRC
CLNACC	RCV000473630.1,