rs794727836

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;TTTTGTC)	5	Hereditary leiomyomatosis and renal cell cancer
(TTTTGTC;TTTTGTC)	0	common in clinvar

Make rs794727836(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241504232

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs794727836
dbSNP (classic)	rs794727836
ClinGen	rs794727836
ebi	rs794727836
HLI	rs794727836
Exac	rs794727836
Gnomad	rs794727836
Varsome	rs794727836
LitVar	rs794727836
Map	rs794727836
PheGenI	rs794727836
Biobank	rs794727836
1000 genomes	rs794727836
hgdp	rs794727836
ensembl	rs794727836
geneview	rs794727836
scholar	rs794727836
google	rs794727836
pharmgkb	rs794727836
gwascentral	rs794727836
openSNP	rs794727836
23andMe	rs794727836
SNPshot	rs794727836
SNPdbe	rs794727836
MSV3d	rs794727836
GWAS Ctlg	rs794727836

Max Magnitude

5

ClinVar
Risk	rs794727836(-;-)
Alt	rs794727836(-;-)
Reference	Rs794727836(TTTTGTC;TTTTGTC)
Significance	Pathogenic
Disease	Hereditary leiomyomatosis and renal cell cancer not provided Fumarase deficiency
Variation	info
Gene	FH
CLNDBN	Hereditary leiomyomatosis and renal cell cancer not provided Fumarase deficiency
Reversed	1
HGVS	NC_000001.10:g.241667532_241667538delGACAAAA
CLNSRC
CLNACC	RCV000179717.1, RCV000199793.2, RCV000477647.1,