rs1060499645

Orientation

minus

Stabilized

minus

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

Make rs1060499645(-;-)

Make rs1060499645(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241497892

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499645
dbSNP (classic)	rs1060499645
ClinGen	rs1060499645
ebi	rs1060499645
HLI	rs1060499645
Exac	rs1060499645
Gnomad	rs1060499645
Varsome	rs1060499645
LitVar	rs1060499645
Map	rs1060499645
PheGenI	rs1060499645
Biobank	rs1060499645
1000 genomes	rs1060499645
hgdp	rs1060499645
ensembl	rs1060499645
geneview	rs1060499645
scholar	rs1060499645
google	rs1060499645
pharmgkb	rs1060499645
gwascentral	rs1060499645
openSNP	rs1060499645
23andMe	rs1060499645
SNPshot	rs1060499645
SNPdbe	rs1060499645
MSV3d	rs1060499645
GWAS Ctlg	rs1060499645

Max Magnitude

0

ClinVar
Risk	rs1060499645(-;-)
Alt	rs1060499645(-;-)
Reference	Rs1060499645(G;G)
Significance	Probable-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.241661192delC
CLNSRC
CLNACC	RCV000445610.1,