rs878855213

Orientation

minus

Stabilized

minus

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

Make rs878855213(-;-)

Make rs878855213(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

17216461

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs878855213
dbSNP (classic)	rs878855213
ClinGen	rs878855213
ebi	rs878855213
HLI	rs878855213
Exac	rs878855213
Gnomad	rs878855213
Varsome	rs878855213
LitVar	rs878855213
Map	rs878855213
PheGenI	rs878855213
Biobank	rs878855213
1000 genomes	rs878855213
hgdp	rs878855213
ensembl	rs878855213
geneview	rs878855213
scholar	rs878855213
google	rs878855213
pharmgkb	rs878855213
gwascentral	rs878855213
openSNP	rs878855213
23andMe	rs878855213
SNPshot	rs878855213
SNPdbe	rs878855213
MSV3d	rs878855213
GWAS Ctlg	rs878855213

Max Magnitude

0

ClinVar
Risk	rs878855213(-;-)
Alt	rs878855213(-;-)
Reference	Rs878855213(A;A)
Significance	Pathogenic
Disease	Multiple fibrofolliculomas not provided
Variation	info
Gene	FLCN LOC101928660
CLNDBN	Multiple fibrofolliculomas not provided
Reversed	1
HGVS	NC_000017.10:g.17119775delT
CLNSRC
CLNACC	RCV000228856.1, RCV000255255.2,