rs1060499642

Orientation

minus

Stabilized

minus

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

Make rs1060499642(G;T)

Make rs1060499642(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241504087

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499642
dbSNP (classic)	rs1060499642
ClinGen	rs1060499642
ebi	rs1060499642
HLI	rs1060499642
Exac	rs1060499642
Gnomad	rs1060499642
Varsome	rs1060499642
LitVar	rs1060499642
Map	rs1060499642
PheGenI	rs1060499642
Biobank	rs1060499642
1000 genomes	rs1060499642
hgdp	rs1060499642
ensembl	rs1060499642
geneview	rs1060499642
scholar	rs1060499642
google	rs1060499642
pharmgkb	rs1060499642
gwascentral	rs1060499642
openSNP	rs1060499642
23andMe	rs1060499642
SNPshot	rs1060499642
SNPdbe	rs1060499642
MSV3d	rs1060499642
GWAS Ctlg	rs1060499642

Max Magnitude

0

ClinVar
Risk	rs1060499642(T;T)
Alt	rs1060499642(T;T)
Reference	Rs1060499642(G;G)
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.241667387C>A
CLNSRC
CLNACC	RCV000445617.1,