rs794727698

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;G)	5	Associated with leiomyomatosis and possibly renal cell cancer
(G;G)	0	common in clinvar

Make rs794727698(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241508786

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs794727698
dbSNP (classic)	rs794727698
ClinGen	rs794727698
ebi	rs794727698
HLI	rs794727698
Exac	rs794727698
Gnomad	rs794727698
Varsome	rs794727698
LitVar	rs794727698
Map	rs794727698
PheGenI	rs794727698
Biobank	rs794727698
1000 genomes	rs794727698
hgdp	rs794727698
ensembl	rs794727698
geneview	rs794727698
scholar	rs794727698
google	rs794727698
pharmgkb	rs794727698
gwascentral	rs794727698
openSNP	rs794727698
23andMe	rs794727698
SNPshot	rs794727698
SNPdbe	rs794727698
MSV3d	rs794727698
GWAS Ctlg	rs794727698

Max Magnitude

5

ClinVar
Risk	rs794727698(C;C)
Alt	rs794727698(C;C)
Reference	Rs794727698(G;G)
Significance	Pathogenic
Disease	Hereditary leiomyomatosis and renal cell cancer
Variation	info
Gene	FH
CLNDBN	Hereditary leiomyomatosis and renal cell cancer
Reversed	1
HGVS	NC_000001.10:g.241672086C>G
CLNSRC
CLNACC	RCV000178715.1,