rs398123168

Orientation

minus

Stabilized

minus

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

Make rs398123168(C;T)

Make rs398123168(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

241504198

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs398123168
dbSNP (classic)	rs398123168
ClinGen	rs398123168
ebi	rs398123168
HLI	rs398123168
Exac	rs398123168
Gnomad	rs398123168
Varsome	rs398123168
LitVar	rs398123168
Map	rs398123168
PheGenI	rs398123168
Biobank	rs398123168
1000 genomes	rs398123168
hgdp	rs398123168
ensembl	rs398123168
geneview	rs398123168
scholar	rs398123168
google	rs398123168
pharmgkb	rs398123168
gwascentral	rs398123168
openSNP	rs398123168
23andMe	rs398123168
SNPshot	rs398123168
SNPdbe	rs398123168
MSV3d	rs398123168
GWAS Ctlg	rs398123168

Max Magnitude

0

ClinVar
Risk	rs398123168(T;T)
Alt	rs398123168(T;T)
Reference	Rs398123168(C;C)
Significance	Other
Disease	not provided Hereditary leiomyomatosis and renal cell cancer
Variation	info
Gene	FH
CLNDBN	not provided Hereditary leiomyomatosis and renal cell cancer
Reversed	1
HGVS	NC_000001.10:g.241667498G>A
CLNSRC	HGMD
CLNACC	RCV000078152.6, RCV000445608.1,