rs754616167

Orientation

plus

Stabilized

plus

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

Make rs754616167(A;A)

Make rs754616167(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

17228105

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs754616167
dbSNP (classic)	rs754616167
ClinGen	rs754616167
ebi	rs754616167
HLI	rs754616167
Exac	rs754616167
Gnomad	rs754616167
Varsome	rs754616167
LitVar	rs754616167
Map	rs754616167
PheGenI	rs754616167
Biobank	rs754616167
1000 genomes	rs754616167
hgdp	rs754616167
ensembl	rs754616167
geneview	rs754616167
scholar	rs754616167
google	rs754616167
pharmgkb	rs754616167
gwascentral	rs754616167
openSNP	rs754616167
23andMe	rs754616167
SNPshot	rs754616167
SNPdbe	rs754616167
MSV3d	rs754616167
GWAS Ctlg	rs754616167

Max Magnitude

0

ClinVar
Risk	rs754616167(A;A)
Alt	rs754616167(A;A)
Reference	Rs754616167(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FLCN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.17131419G>T
CLNSRC
CLNACC	RCV000492609.1,