rs1060499641

Orientation

minus

Stabilized

minus

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

Make rs1060499641(-;-)

Make rs1060499641(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241504109

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499641
dbSNP (classic)	rs1060499641
ClinGen	rs1060499641
ebi	rs1060499641
HLI	rs1060499641
Exac	rs1060499641
Gnomad	rs1060499641
Varsome	rs1060499641
LitVar	rs1060499641
Map	rs1060499641
PheGenI	rs1060499641
Biobank	rs1060499641
1000 genomes	rs1060499641
hgdp	rs1060499641
ensembl	rs1060499641
geneview	rs1060499641
scholar	rs1060499641
google	rs1060499641
pharmgkb	rs1060499641
gwascentral	rs1060499641
openSNP	rs1060499641
23andMe	rs1060499641
SNPshot	rs1060499641
SNPdbe	rs1060499641
MSV3d	rs1060499641
GWAS Ctlg	rs1060499641

Max Magnitude

0

ClinVar
Risk	rs1060499641(-;-)
Alt	rs1060499641(-;-)
Reference	Rs1060499641(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.241667409delA
CLNSRC
CLNACC	RCV000445598.1,