rs398123167

Orientation

minus

Stabilized

minus

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

Make rs398123167(C;T)

Make rs398123167(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

241506147

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs398123167
dbSNP (classic)	rs398123167
ClinGen	rs398123167
ebi	rs398123167
HLI	rs398123167
Exac	rs398123167
Gnomad	rs398123167
Varsome	rs398123167
LitVar	rs398123167
Map	rs398123167
PheGenI	rs398123167
Biobank	rs398123167
1000 genomes	rs398123167
hgdp	rs398123167
ensembl	rs398123167
geneview	rs398123167
scholar	rs398123167
google	rs398123167
pharmgkb	rs398123167
gwascentral	rs398123167
openSNP	rs398123167
23andMe	rs398123167
SNPshot	rs398123167
SNPdbe	rs398123167
MSV3d	rs398123167
GWAS Ctlg	rs398123167

Max Magnitude

0

ClinVar
Risk	rs398123167(T;T)
Alt	rs398123167(T;T)
Reference	Rs398123167(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241669447G>A
CLNSRC	ClinVar Emory University
CLNACC	RCV000078151.4,