rs863223999

Orientation

minus

Stabilized

minus

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

Make rs863223999(A;A)

Make rs863223999(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241506002

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223999
dbSNP (classic)	rs863223999
ClinGen	rs863223999
ebi	rs863223999
HLI	rs863223999
Exac	rs863223999
Gnomad	rs863223999
Varsome	rs863223999
LitVar	rs863223999
Map	rs863223999
PheGenI	rs863223999
Biobank	rs863223999
1000 genomes	rs863223999
hgdp	rs863223999
ensembl	rs863223999
geneview	rs863223999
scholar	rs863223999
google	rs863223999
pharmgkb	rs863223999
gwascentral	rs863223999
openSNP	rs863223999
23andMe	rs863223999
SNPshot	rs863223999
SNPdbe	rs863223999
MSV3d	rs863223999
GWAS Ctlg	rs863223999

Max Magnitude

0

ClinVar
Risk	rs863223999(A;A)
Alt	rs863223999(A;A)
Reference	Rs863223999(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241669302C>T
CLNSRC
CLNACC	RCV000195849.1,