rs863224011

Orientation

minus

Stabilized

minus

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

Make rs863224011(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241517317

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863224011
dbSNP (classic)	rs863224011
ClinGen	rs863224011
ebi	rs863224011
HLI	rs863224011
Exac	rs863224011
Gnomad	rs863224011
Varsome	rs863224011
LitVar	rs863224011
Map	rs863224011
PheGenI	rs863224011
Biobank	rs863224011
1000 genomes	rs863224011
hgdp	rs863224011
ensembl	rs863224011
geneview	rs863224011
scholar	rs863224011
google	rs863224011
pharmgkb	rs863224011
gwascentral	rs863224011
openSNP	rs863224011
23andMe	rs863224011
SNPshot	rs863224011
SNPdbe	rs863224011
MSV3d	rs863224011
GWAS Ctlg	rs863224011

Max Magnitude

5

ClinVar
Risk	rs863224011(A;A)
Alt	rs863224011(A;A)
Reference	Rs863224011(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.241680617C>T
CLNSRC
CLNACC	RCV000445590.1,