rs863223989

Orientation

minus

Stabilized

minus

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

Make rs863223989(-;-)

Make rs863223989(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241500564

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223989
dbSNP (classic)	rs863223989
ClinGen	rs863223989
ebi	rs863223989
HLI	rs863223989
Exac	rs863223989
Gnomad	rs863223989
Varsome	rs863223989
LitVar	rs863223989
Map	rs863223989
PheGenI	rs863223989
Biobank	rs863223989
1000 genomes	rs863223989
hgdp	rs863223989
ensembl	rs863223989
geneview	rs863223989
scholar	rs863223989
google	rs863223989
pharmgkb	rs863223989
gwascentral	rs863223989
openSNP	rs863223989
23andMe	rs863223989
SNPshot	rs863223989
SNPdbe	rs863223989
MSV3d	rs863223989
GWAS Ctlg	rs863223989

Max Magnitude

0

ClinVar
Risk	rs863223989(-;-)
Alt	rs863223989(-;-)
Reference	Rs863223989(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241663864delC
CLNSRC
CLNACC	RCV000196430.1,