rs863223967

Orientation

minus

Stabilized

minus

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

Make rs863223967(A;G)

Make rs863223967(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241508653

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223967
dbSNP (classic)	rs863223967
ClinGen	rs863223967
ebi	rs863223967
HLI	rs863223967
Exac	rs863223967
Gnomad	rs863223967
Varsome	rs863223967
LitVar	rs863223967
Map	rs863223967
PheGenI	rs863223967
Biobank	rs863223967
1000 genomes	rs863223967
hgdp	rs863223967
ensembl	rs863223967
geneview	rs863223967
scholar	rs863223967
google	rs863223967
pharmgkb	rs863223967
gwascentral	rs863223967
openSNP	rs863223967
23andMe	rs863223967
SNPshot	rs863223967
SNPdbe	rs863223967
MSV3d	rs863223967
GWAS Ctlg	rs863223967

Max Magnitude

0

ClinVar
Risk	rs863223967(G;G)
Alt	rs863223967(G;G)
Reference	Rs863223967(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241671953T>C
CLNSRC
CLNACC	RCV000198721.1,