rs1064793128

Orientation

minus

Stabilized

minus

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

Chromosome

17

Position

17215237

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs1064793128
dbSNP (classic)	rs1064793128
ClinGen	rs1064793128
ebi	rs1064793128
HLI	rs1064793128
Exac	rs1064793128
Gnomad	rs1064793128
Varsome	rs1064793128
LitVar	rs1064793128
Map	rs1064793128
PheGenI	rs1064793128
Biobank	rs1064793128
1000 genomes	rs1064793128
hgdp	rs1064793128
ensembl	rs1064793128
geneview	rs1064793128
scholar	rs1064793128
google	rs1064793128
pharmgkb	rs1064793128
gwascentral	rs1064793128
openSNP	rs1064793128
23andMe	rs1064793128
SNPshot	rs1064793128
SNPdbe	rs1064793128
MSV3d	rs1064793128
GWAS Ctlg	rs1064793128

Max Magnitude

0

ClinVar
Risk	rs1064793128(-;-)
Alt	rs1064793128(-;-)
Reference	Rs1064793128(TC;TC)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	FLCN
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.17118551_17118552delGA
CLNSRC
CLNACC	RCV000485073.1, RCV000492502.1,