rs1060499643

Orientation

minus

Stabilized

minus

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

Make rs1060499643(A;G)

Make rs1060499643(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241502561

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499643
dbSNP (classic)	rs1060499643
ClinGen	rs1060499643
ebi	rs1060499643
HLI	rs1060499643
Exac	rs1060499643
Gnomad	rs1060499643
Varsome	rs1060499643
LitVar	rs1060499643
Map	rs1060499643
PheGenI	rs1060499643
Biobank	rs1060499643
1000 genomes	rs1060499643
hgdp	rs1060499643
ensembl	rs1060499643
geneview	rs1060499643
scholar	rs1060499643
google	rs1060499643
pharmgkb	rs1060499643
gwascentral	rs1060499643
openSNP	rs1060499643
23andMe	rs1060499643
SNPshot	rs1060499643
SNPdbe	rs1060499643
MSV3d	rs1060499643
GWAS Ctlg	rs1060499643

Max Magnitude

0

ClinVar
Risk	rs1060499643(G;G)
Alt	rs1060499643(G;G)
Reference	Rs1060499643(A;A)
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.241665861T>C
CLNSRC
CLNACC	RCV000445626.1,