rs1060499634

Orientation

minus

Stabilized

minus

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

Make rs1060499634(-;-)

Make rs1060499634(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241511998

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499634
dbSNP (classic)	rs1060499634
ClinGen	rs1060499634
ebi	rs1060499634
HLI	rs1060499634
Exac	rs1060499634
Gnomad	rs1060499634
Varsome	rs1060499634
LitVar	rs1060499634
Map	rs1060499634
PheGenI	rs1060499634
Biobank	rs1060499634
1000 genomes	rs1060499634
hgdp	rs1060499634
ensembl	rs1060499634
geneview	rs1060499634
scholar	rs1060499634
google	rs1060499634
pharmgkb	rs1060499634
gwascentral	rs1060499634
openSNP	rs1060499634
23andMe	rs1060499634
SNPshot	rs1060499634
SNPdbe	rs1060499634
MSV3d	rs1060499634
GWAS Ctlg	rs1060499634

Max Magnitude

0

ClinVar
Risk	rs1060499634(-;-)
Alt	rs1060499634(-;-)
Reference	Rs1060499634(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.241675298delA
CLNSRC
CLNACC	RCV000445619.1,