rs876658569

Orientation

minus

Stabilized

minus

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

Make rs876658569(-;-)

Make rs876658569(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

241513665

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs876658569
dbSNP (classic)	rs876658569
ClinGen	rs876658569
ebi	rs876658569
HLI	rs876658569
Exac	rs876658569
Gnomad	rs876658569
Varsome	rs876658569
LitVar	rs876658569
Map	rs876658569
PheGenI	rs876658569
Biobank	rs876658569
1000 genomes	rs876658569
hgdp	rs876658569
ensembl	rs876658569
geneview	rs876658569
scholar	rs876658569
google	rs876658569
pharmgkb	rs876658569
gwascentral	rs876658569
openSNP	rs876658569
23andMe	rs876658569
SNPshot	rs876658569
SNPdbe	rs876658569
MSV3d	rs876658569
GWAS Ctlg	rs876658569

Max Magnitude

0

ClinVar
Risk	rs876658569(-;-)
Alt	rs876658569(-;-)
Reference	Rs876658569(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	FH
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.241676965delC
CLNSRC
CLNACC	RCV000213630.1, RCV000275674.1,