rs767671406

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GAG;GAG)	0	common in clinvar
(I;I)	0	common genotype

Make rs767671406(-;-)

Make rs767671406(-;GAG)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

17216506

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs767671406
dbSNP (classic)	rs767671406
ClinGen	rs767671406
ebi	rs767671406
HLI	rs767671406
Exac	rs767671406
Gnomad	rs767671406
Varsome	rs767671406
LitVar	rs767671406
Map	rs767671406
PheGenI	rs767671406
Biobank	rs767671406
1000 genomes	rs767671406
hgdp	rs767671406
ensembl	rs767671406
geneview	rs767671406
scholar	rs767671406
google	rs767671406
pharmgkb	rs767671406
gwascentral	rs767671406
openSNP	rs767671406
23andMe	rs767671406
SNPshot	rs767671406
SNPdbe	rs767671406
MSV3d	rs767671406
GWAS Ctlg	rs767671406

Max Magnitude

0

ClinVar
Risk	rs767671406(-;-)
Alt	rs767671406(-;-)
Reference	Rs767671406(GAG;GAG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not specified Multiple fibrofolliculomas not provided
Variation	info
Gene	FLCN LOC101928660
CLNDBN	Hereditary cancer-predisposing syndrome not specified Multiple fibrofolliculomas not provided
Reversed	0
HGVS	NC_000017.10:g.17119820_17119822delGAG
CLNSRC
CLNACC	RCV000217238.1, RCV000217604.1, RCV000239690.1, RCV000255836.2,