rs863223966

Orientation

minus

Stabilized

minus

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

Make rs863223966(A;G)

Make rs863223966(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241504057

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223966
dbSNP (classic)	rs863223966
ClinGen	rs863223966
ebi	rs863223966
HLI	rs863223966
Exac	rs863223966
Gnomad	rs863223966
Varsome	rs863223966
LitVar	rs863223966
Map	rs863223966
PheGenI	rs863223966
Biobank	rs863223966
1000 genomes	rs863223966
hgdp	rs863223966
ensembl	rs863223966
geneview	rs863223966
scholar	rs863223966
google	rs863223966
pharmgkb	rs863223966
gwascentral	rs863223966
openSNP	rs863223966
23andMe	rs863223966
SNPshot	rs863223966
SNPdbe	rs863223966
MSV3d	rs863223966
GWAS Ctlg	rs863223966

Max Magnitude

0

ClinVar
Risk	rs863223966(G;G)
Alt	rs863223966(G;G)
Reference	Rs863223966(A;A)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome Hereditary leiomyomatosis and renal cell cancer
Variation	info
Gene	FH
CLNDBN	not provided Hereditary cancer-predisposing syndrome Hereditary leiomyomatosis and renal cell cancer
Reversed	1
HGVS	NC_000001.10:g.241667357T>C
CLNSRC
CLNACC	RCV000196179.3, RCV000220270.2, RCV000445606.1,