rs1057518147

Orientation

minus

Stabilized

minus

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

Make rs1057518147(-;-)

Make rs1057518147(-;AT)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

17227896

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs1057518147
dbSNP (classic)	rs1057518147
ClinGen	rs1057518147
ebi	rs1057518147
HLI	rs1057518147
Exac	rs1057518147
Gnomad	rs1057518147
Varsome	rs1057518147
LitVar	rs1057518147
Map	rs1057518147
PheGenI	rs1057518147
Biobank	rs1057518147
1000 genomes	rs1057518147
hgdp	rs1057518147
ensembl	rs1057518147
geneview	rs1057518147
scholar	rs1057518147
google	rs1057518147
pharmgkb	rs1057518147
gwascentral	rs1057518147
openSNP	rs1057518147
23andMe	rs1057518147
SNPshot	rs1057518147
SNPdbe	rs1057518147
MSV3d	rs1057518147
GWAS Ctlg	rs1057518147

Max Magnitude

0

ClinVar
Risk	rs1057518147(-;-)
Alt	rs1057518147(-;-)
Reference	Rs1057518147(AT;AT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLCN
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.17131210_17131211delAT
CLNSRC
CLNACC	RCV000413452.1,