rs398124539

Orientation

minus

Stabilized

minus

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

Make rs398124539(-;TG)

Make rs398124539(TG;TG)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17221578

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124539
dbSNP (classic)	rs398124539
ClinGen	rs398124539
ebi	rs398124539
HLI	rs398124539
Exac	rs398124539
Gnomad	rs398124539
Varsome	rs398124539
LitVar	rs398124539
Map	rs398124539
PheGenI	rs398124539
Biobank	rs398124539
1000 genomes	rs398124539
hgdp	rs398124539
ensembl	rs398124539
geneview	rs398124539
scholar	rs398124539
google	rs398124539
pharmgkb	rs398124539
gwascentral	rs398124539
openSNP	rs398124539
23andMe	rs398124539
SNPshot	rs398124539
SNPdbe	rs398124539
MSV3d	rs398124539
GWAS Ctlg	rs398124539

Max Magnitude

0

ClinVar
Risk	rs398124539(TG;TG)
Alt	rs398124539(TG;TG)
Reference	Rs398124539(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLCN
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.17124893_17124894dupCA
CLNSRC	ClinVar
CLNACC	RCV000082642.3,