rs137852930

Orientation

minus

Stabilized

minus

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

Make rs137852930(C;G)

Make rs137852930(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17227902

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs137852930
dbSNP (classic)	rs137852930
ClinGen	rs137852930
ebi	rs137852930
HLI	rs137852930
Exac	rs137852930
Gnomad	rs137852930
Varsome	rs137852930
LitVar	rs137852930
Map	rs137852930
PheGenI	rs137852930
Biobank	rs137852930
1000 genomes	rs137852930
hgdp	rs137852930
ensembl	rs137852930
geneview	rs137852930
scholar	rs137852930
google	rs137852930
pharmgkb	rs137852930
gwascentral	rs137852930
openSNP	rs137852930
23andMe	rs137852930
SNPshot	rs137852930
SNPdbe	rs137852930
MSV3d	rs137852930
GWAS Ctlg	rs137852930

Max Magnitude

0

OMIM	607273
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137852930(G;G)
Alt	rs137852930(G;G)
Reference	Rs137852930(C;C)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	FLCN
CLNDBN	Carcinoma of colon
Reversed	1
HGVS	NC_000017.10:g.17131216G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003536.5,