rs863224005

Orientation

minus

Stabilized

minus

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

Make rs863224005(A;G)

Make rs863224005(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241502567

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863224005
dbSNP (classic)	rs863224005
ClinGen	rs863224005
ebi	rs863224005
HLI	rs863224005
Exac	rs863224005
Gnomad	rs863224005
Varsome	rs863224005
LitVar	rs863224005
Map	rs863224005
PheGenI	rs863224005
Biobank	rs863224005
1000 genomes	rs863224005
hgdp	rs863224005
ensembl	rs863224005
geneview	rs863224005
scholar	rs863224005
google	rs863224005
pharmgkb	rs863224005
gwascentral	rs863224005
openSNP	rs863224005
23andMe	rs863224005
SNPshot	rs863224005
SNPdbe	rs863224005
MSV3d	rs863224005
GWAS Ctlg	rs863224005

Max Magnitude

0

ClinVar
Risk	rs863224005(G;G)
Alt	rs863224005(G;G)
Reference	Rs863224005(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241665867T>C
CLNSRC
CLNACC	RCV000197014.1,