rs398124530

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	5	Birt-Hogg-Dube Syndrome
(G;G)	0	common in clinvar

Make rs398124530(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17214990

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124530
dbSNP (classic)	rs398124530
ClinGen	rs398124530
ebi	rs398124530
HLI	rs398124530
Exac	rs398124530
Gnomad	rs398124530
Varsome	rs398124530
LitVar	rs398124530
Map	rs398124530
PheGenI	rs398124530
Biobank	rs398124530
1000 genomes	rs398124530
hgdp	rs398124530
ensembl	rs398124530
geneview	rs398124530
scholar	rs398124530
google	rs398124530
pharmgkb	rs398124530
gwascentral	rs398124530
openSNP	rs398124530
23andMe	rs398124530
SNPshot	rs398124530
SNPdbe	rs398124530
MSV3d	rs398124530
GWAS Ctlg	rs398124530

Max Magnitude

5

ClinVar
Risk	rs398124530(A;A)
Alt	rs398124530(A;A)
Reference	Rs398124530(G;G)
Significance	Pathogenic
Disease	not provided Multiple fibrofolliculomas
Variation	info
Gene	FLCN LOC101928660
CLNDBN	not provided Multiple fibrofolliculomas
Reversed	1
HGVS	NC_000017.10:g.17118304C>T
CLNSRC	HGMD
CLNACC	RCV000082630.4, RCV000239664.1,