rs863223975

Orientation

minus

Stabilized

minus

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

Make rs863223975(A;C)

Make rs863223975(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241500511

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223975
dbSNP (classic)	rs863223975
ClinGen	rs863223975
ebi	rs863223975
HLI	rs863223975
Exac	rs863223975
Gnomad	rs863223975
Varsome	rs863223975
LitVar	rs863223975
Map	rs863223975
PheGenI	rs863223975
Biobank	rs863223975
1000 genomes	rs863223975
hgdp	rs863223975
ensembl	rs863223975
geneview	rs863223975
scholar	rs863223975
google	rs863223975
pharmgkb	rs863223975
gwascentral	rs863223975
openSNP	rs863223975
23andMe	rs863223975
SNPshot	rs863223975
SNPdbe	rs863223975
MSV3d	rs863223975
GWAS Ctlg	rs863223975

Max Magnitude

0

ClinVar
Risk	rs863223975(C;C)
Alt	rs863223975(C;C)
Reference	Rs863223975(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241663811T>G
CLNSRC
CLNACC	RCV000196513.1,