rs863223976

Orientation

minus

Stabilized

minus

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

Make rs863223976(G;T)

Make rs863223976(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241500500

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223976
dbSNP (classic)	rs863223976
ClinGen	rs863223976
ebi	rs863223976
HLI	rs863223976
Exac	rs863223976
Gnomad	rs863223976
Varsome	rs863223976
LitVar	rs863223976
Map	rs863223976
PheGenI	rs863223976
Biobank	rs863223976
1000 genomes	rs863223976
hgdp	rs863223976
ensembl	rs863223976
geneview	rs863223976
scholar	rs863223976
google	rs863223976
pharmgkb	rs863223976
gwascentral	rs863223976
openSNP	rs863223976
23andMe	rs863223976
SNPshot	rs863223976
SNPdbe	rs863223976
MSV3d	rs863223976
GWAS Ctlg	rs863223976

Max Magnitude

0

ClinVar
Risk	rs863223976(T;T)
Alt	rs863223976(T;T)
Reference	Rs863223976(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241663800C>A
CLNSRC
CLNACC	RCV000198349.1,