rs863224003

Orientation

minus

Stabilized

minus

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

Make rs863224003(G;G)

Make rs863224003(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241504185

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863224003
dbSNP (classic)	rs863224003
ClinGen	rs863224003
ebi	rs863224003
HLI	rs863224003
Exac	rs863224003
Gnomad	rs863224003
Varsome	rs863224003
LitVar	rs863224003
Map	rs863224003
PheGenI	rs863224003
Biobank	rs863224003
1000 genomes	rs863224003
hgdp	rs863224003
ensembl	rs863224003
geneview	rs863224003
scholar	rs863224003
google	rs863224003
pharmgkb	rs863224003
gwascentral	rs863224003
openSNP	rs863224003
23andMe	rs863224003
SNPshot	rs863224003
SNPdbe	rs863224003
MSV3d	rs863224003
GWAS Ctlg	rs863224003

Max Magnitude

0

ClinVar
Risk	rs863224003(G;G)
Alt	rs863224003(G;G)
Reference	Rs863224003(T;T)
Significance	Probable-Pathogenic
Disease	not specified Hereditary leiomyomatosis and renal cell cancer
Variation	info
Gene	FH
CLNDBN	not specified Hereditary leiomyomatosis and renal cell cancer
Reversed	1
HGVS	NC_000001.10:g.241667485A>C
CLNSRC
CLNACC	RCV000196089.3, RCV000445631.1,