rs863223972

Orientation

minus

Stabilized

minus

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

Make rs863223972(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241504143

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223972
dbSNP (classic)	rs863223972
ClinGen	rs863223972
ebi	rs863223972
HLI	rs863223972
Exac	rs863223972
Gnomad	rs863223972
Varsome	rs863223972
LitVar	rs863223972
Map	rs863223972
PheGenI	rs863223972
Biobank	rs863223972
1000 genomes	rs863223972
hgdp	rs863223972
ensembl	rs863223972
geneview	rs863223972
scholar	rs863223972
google	rs863223972
pharmgkb	rs863223972
gwascentral	rs863223972
openSNP	rs863223972
23andMe	rs863223972
SNPshot	rs863223972
SNPdbe	rs863223972
MSV3d	rs863223972
GWAS Ctlg	rs863223972

Max Magnitude

5

ClinVar
Risk	rs863223972(G;G)
Alt	rs863223972(G;G)
Reference	Rs863223972(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FH
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000001.10:g.241667443A>C
CLNSRC
CLNACC	RCV000493913.1,