rs1060502371

Orientation

minus

Stabilized

minus

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

Make rs1060502371(-;-)

Make rs1060502371(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

17227899

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs1060502371
dbSNP (classic)	rs1060502371
ClinGen	rs1060502371
ebi	rs1060502371
HLI	rs1060502371
Exac	rs1060502371
Gnomad	rs1060502371
Varsome	rs1060502371
LitVar	rs1060502371
Map	rs1060502371
PheGenI	rs1060502371
Biobank	rs1060502371
1000 genomes	rs1060502371
hgdp	rs1060502371
ensembl	rs1060502371
geneview	rs1060502371
scholar	rs1060502371
google	rs1060502371
pharmgkb	rs1060502371
gwascentral	rs1060502371
openSNP	rs1060502371
23andMe	rs1060502371
SNPshot	rs1060502371
SNPdbe	rs1060502371
MSV3d	rs1060502371
GWAS Ctlg	rs1060502371

Max Magnitude

0

ClinVar
Risk	rs1060502371(-;-)
Alt	rs1060502371(-;-)
Reference	Rs1060502371(A;A)
Significance	Pathogenic
Disease	Multiple fibrofolliculomas
Variation	info
Gene	FLCN
CLNDBN	Multiple fibrofolliculomas
Reversed	1
HGVS	NC_000017.10:g.17131213delT
CLNSRC
CLNACC	RCV000461846.1,