rs863223991

Orientation

minus

Stabilized

minus

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

Make rs863223991(-;-)

Make rs863223991(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241500469

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223991
dbSNP (classic)	rs863223991
ClinGen	rs863223991
ebi	rs863223991
HLI	rs863223991
Exac	rs863223991
Gnomad	rs863223991
Varsome	rs863223991
LitVar	rs863223991
Map	rs863223991
PheGenI	rs863223991
Biobank	rs863223991
1000 genomes	rs863223991
hgdp	rs863223991
ensembl	rs863223991
geneview	rs863223991
scholar	rs863223991
google	rs863223991
pharmgkb	rs863223991
gwascentral	rs863223991
openSNP	rs863223991
23andMe	rs863223991
SNPshot	rs863223991
SNPdbe	rs863223991
MSV3d	rs863223991
GWAS Ctlg	rs863223991

Max Magnitude

0

ClinVar
Risk	rs863223991(-;-)
Alt	rs863223991(-;-)
Reference	Rs863223991(CT;CT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241663769_241663770delAG
CLNSRC
CLNACC	RCV000197139.1,