rs1060499638

Orientation

minus

Stabilized

minus

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

Make rs1060499638(C;C)

Make rs1060499638(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241506087

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499638
dbSNP (classic)	rs1060499638
ClinGen	rs1060499638
ebi	rs1060499638
HLI	rs1060499638
Exac	rs1060499638
Gnomad	rs1060499638
Varsome	rs1060499638
LitVar	rs1060499638
Map	rs1060499638
PheGenI	rs1060499638
Biobank	rs1060499638
1000 genomes	rs1060499638
hgdp	rs1060499638
ensembl	rs1060499638
geneview	rs1060499638
scholar	rs1060499638
google	rs1060499638
pharmgkb	rs1060499638
gwascentral	rs1060499638
openSNP	rs1060499638
23andMe	rs1060499638
SNPshot	rs1060499638
SNPdbe	rs1060499638
MSV3d	rs1060499638
GWAS Ctlg	rs1060499638

Max Magnitude

0

ClinVar
Risk	rs1060499638(C;C)
Alt	rs1060499638(C;C)
Reference	Rs1060499638(G;G)
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.241669387C>G
CLNSRC
CLNACC	RCV000445594.1,