rs1060499644

Orientation

minus

Stabilized

minus

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

Make rs1060499644(-;-)

Make rs1060499644(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241502470

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499644
dbSNP (classic)	rs1060499644
ClinGen	rs1060499644
ebi	rs1060499644
HLI	rs1060499644
Exac	rs1060499644
Gnomad	rs1060499644
Varsome	rs1060499644
LitVar	rs1060499644
Map	rs1060499644
PheGenI	rs1060499644
Biobank	rs1060499644
1000 genomes	rs1060499644
hgdp	rs1060499644
ensembl	rs1060499644
geneview	rs1060499644
scholar	rs1060499644
google	rs1060499644
pharmgkb	rs1060499644
gwascentral	rs1060499644
openSNP	rs1060499644
23andMe	rs1060499644
SNPshot	rs1060499644
SNPdbe	rs1060499644
MSV3d	rs1060499644
GWAS Ctlg	rs1060499644

Max Magnitude

0

ClinVar
Risk	rs1060499644(-;-)
Alt	rs1060499644(-;-)
Reference	Rs1060499644(T;T)
Significance	Pathogenic
Disease	Hereditary leiomyomatosis and renal cell cancer
Variation	info
Gene	FH
CLNDBN	Hereditary leiomyomatosis and renal cell cancer
Reversed	1
HGVS	NC_000001.10:g.241665770delA
CLNSRC
CLNACC	RCV000445613.1,