rs561236067

Orientation

plus

Stabilized

plus

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

Make rs561236067(A;A)

Make rs561236067(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

17216453

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs561236067
dbSNP (classic)	rs561236067
ClinGen	rs561236067
ebi	rs561236067
HLI	rs561236067
Exac	rs561236067
Gnomad	rs561236067
Varsome	rs561236067
LitVar	rs561236067
Map	rs561236067
PheGenI	rs561236067
Biobank	rs561236067
1000 genomes	rs561236067
hgdp	rs561236067
ensembl	rs561236067
geneview	rs561236067
scholar	rs561236067
google	rs561236067
pharmgkb	rs561236067
gwascentral	rs561236067
openSNP	rs561236067
23andMe	rs561236067
SNPshot	rs561236067
SNPdbe	rs561236067
MSV3d	rs561236067
GWAS Ctlg	rs561236067

Max Magnitude

0

ClinVar
Risk	rs561236067(A;A) rs561236067(C;C) rs561236067(T;T)
Alt	rs561236067(A;A) rs561236067(C;C) rs561236067(T;T)
Reference	Rs561236067(G;G)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	FLCN LOC101928660
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000017.10:g.17119767G>A; NC_000017.10:g.17119767G>C; NC_000017.10:g.17119767G>T
CLNSRC
CLNACC	RCV000436342.1, RCV000294917.1, RCV000420603.1,