rs398124523

Orientation

minus

Stabilized

minus

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

Make rs398124523(C;T)

Make rs398124523(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17219021

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124523
dbSNP (classic)	rs398124523
ClinGen	rs398124523
ebi	rs398124523
HLI	rs398124523
Exac	rs398124523
Gnomad	rs398124523
Varsome	rs398124523
LitVar	rs398124523
Map	rs398124523
PheGenI	rs398124523
Biobank	rs398124523
1000 genomes	rs398124523
hgdp	rs398124523
ensembl	rs398124523
geneview	rs398124523
scholar	rs398124523
google	rs398124523
pharmgkb	rs398124523
gwascentral	rs398124523
openSNP	rs398124523
23andMe	rs398124523
SNPshot	rs398124523
SNPdbe	rs398124523
MSV3d	rs398124523
GWAS Ctlg	rs398124523

Max Magnitude

0

ClinVar
Risk	rs398124523(T;T)
Alt	rs398124523(T;T)
Reference	Rs398124523(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLCN
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.17122335G>A
CLNSRC	ClinVar Emory University
CLNACC	RCV000082617.4,