rs398124532

Orientation

minus

Stabilized

minus

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

Make rs398124532(C;T)

Make rs398124532(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17213798

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124532
dbSNP (classic)	rs398124532
ClinGen	rs398124532
ebi	rs398124532
HLI	rs398124532
Exac	rs398124532
Gnomad	rs398124532
Varsome	rs398124532
LitVar	rs398124532
Map	rs398124532
PheGenI	rs398124532
Biobank	rs398124532
1000 genomes	rs398124532
hgdp	rs398124532
ensembl	rs398124532
geneview	rs398124532
scholar	rs398124532
google	rs398124532
pharmgkb	rs398124532
gwascentral	rs398124532
openSNP	rs398124532
23andMe	rs398124532
SNPshot	rs398124532
SNPdbe	rs398124532
MSV3d	rs398124532
GWAS Ctlg	rs398124532

Max Magnitude

0

ClinVar
Risk	rs398124532(G;G) rs398124532(T;T)
Alt	rs398124532(G;G) rs398124532(T;T)
Reference	Rs398124532(C;C)
Significance	Other
Disease	not provided
Variation	info
Gene	FLCN LOC101928660
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.17117112G>A
CLNSRC	HGMD
CLNACC	RCV000082632.4,