rs1060499635

Orientation

minus

Stabilized

minus

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

Make rs1060499635(-;-)

Make rs1060499635(-;CAGCAA)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241508758

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499635
dbSNP (classic)	rs1060499635
ClinGen	rs1060499635
ebi	rs1060499635
HLI	rs1060499635
Exac	rs1060499635
Gnomad	rs1060499635
Varsome	rs1060499635
LitVar	rs1060499635
Map	rs1060499635
PheGenI	rs1060499635
Biobank	rs1060499635
1000 genomes	rs1060499635
hgdp	rs1060499635
ensembl	rs1060499635
geneview	rs1060499635
scholar	rs1060499635
google	rs1060499635
pharmgkb	rs1060499635
gwascentral	rs1060499635
openSNP	rs1060499635
23andMe	rs1060499635
SNPshot	rs1060499635
SNPdbe	rs1060499635
MSV3d	rs1060499635
GWAS Ctlg	rs1060499635

Max Magnitude

0

ClinVar
Risk	rs1060499635(-;-)
Alt	rs1060499635(-;-)
Reference	Rs1060499635(CAGCAA;CAGCAA)
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.241672058_241672063delTTGCTG
CLNSRC
CLNACC	RCV000445627.1,