rs398124540

Orientation

minus

Stabilized

minus

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

Make rs398124540(-;C)

Make rs398124540(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17228054

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124540
dbSNP (classic)	rs398124540
ClinGen	rs398124540
ebi	rs398124540
HLI	rs398124540
Exac	rs398124540
Gnomad	rs398124540
Varsome	rs398124540
LitVar	rs398124540
Map	rs398124540
PheGenI	rs398124540
Biobank	rs398124540
1000 genomes	rs398124540
hgdp	rs398124540
ensembl	rs398124540
geneview	rs398124540
scholar	rs398124540
google	rs398124540
pharmgkb	rs398124540
gwascentral	rs398124540
openSNP	rs398124540
23andMe	rs398124540
SNPshot	rs398124540
SNPdbe	rs398124540
MSV3d	rs398124540
GWAS Ctlg	rs398124540

Max Magnitude

0

ClinVar
Risk	rs398124540(C;C)
Alt	rs398124540(C;C)
Reference	Rs398124540(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLCN
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.17131369dupG
CLNSRC	ClinVar
CLNACC	RCV000082643.3,