rs398124535

Orientation

minus

Stabilized

minus

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

Make rs398124535(CAC;CAC)

Make rs398124535(CAC;GT)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17226252

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124535
dbSNP (classic)	rs398124535
ClinGen	rs398124535
ebi	rs398124535
HLI	rs398124535
Exac	rs398124535
Gnomad	rs398124535
Varsome	rs398124535
LitVar	rs398124535
Map	rs398124535
PheGenI	rs398124535
Biobank	rs398124535
1000 genomes	rs398124535
hgdp	rs398124535
ensembl	rs398124535
geneview	rs398124535
scholar	rs398124535
google	rs398124535
pharmgkb	rs398124535
gwascentral	rs398124535
openSNP	rs398124535
23andMe	rs398124535
SNPshot	rs398124535
SNPdbe	rs398124535
MSV3d	rs398124535
GWAS Ctlg	rs398124535

Max Magnitude

0

ClinVar
Risk	rs398124535(CAC;CAC)
Alt	rs398124535(CAC;CAC)
Reference	Rs398124535(GT;GT)
Significance	Pathogenic
Disease	not provided Multiple fibrofolliculomas Hereditary cancer-predisposing syndrome
Variation	info
Gene	FLCN
CLNDBN	not provided Multiple fibrofolliculomas Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.17129566_17129567delACinsGTG
CLNSRC	HGMD
CLNACC	RCV000082635.4, RCV000239674.1, RCV000492373.1,