rs1057520528

Orientation

minus

Stabilized

minus

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

Make rs1057520528(A;G)

Make rs1057520528(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

17216505

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs1057520528
dbSNP (classic)	rs1057520528
ClinGen	rs1057520528
ebi	rs1057520528
HLI	rs1057520528
Exac	rs1057520528
Gnomad	rs1057520528
Varsome	rs1057520528
LitVar	rs1057520528
Map	rs1057520528
PheGenI	rs1057520528
Biobank	rs1057520528
1000 genomes	rs1057520528
hgdp	rs1057520528
ensembl	rs1057520528
geneview	rs1057520528
scholar	rs1057520528
google	rs1057520528
pharmgkb	rs1057520528
gwascentral	rs1057520528
openSNP	rs1057520528
23andMe	rs1057520528
SNPshot	rs1057520528
SNPdbe	rs1057520528
MSV3d	rs1057520528
GWAS Ctlg	rs1057520528

Max Magnitude

0

ClinVar
Risk	rs1057520528(G;G)
Alt	rs1057520528(G;G)
Reference	Rs1057520528(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLCN
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.17119819T>C
CLNSRC
CLNACC	RCV000444206.1,