rs1060499637

Orientation

minus

Stabilized

minus

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

Make rs1060499637(-;-)

Make rs1060499637(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241506099

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499637
dbSNP (classic)	rs1060499637
ClinGen	rs1060499637
ebi	rs1060499637
HLI	rs1060499637
Exac	rs1060499637
Gnomad	rs1060499637
Varsome	rs1060499637
LitVar	rs1060499637
Map	rs1060499637
PheGenI	rs1060499637
Biobank	rs1060499637
1000 genomes	rs1060499637
hgdp	rs1060499637
ensembl	rs1060499637
geneview	rs1060499637
scholar	rs1060499637
google	rs1060499637
pharmgkb	rs1060499637
gwascentral	rs1060499637
openSNP	rs1060499637
23andMe	rs1060499637
SNPshot	rs1060499637
SNPdbe	rs1060499637
MSV3d	rs1060499637
GWAS Ctlg	rs1060499637

Max Magnitude

0

ClinVar
Risk	rs1060499637(-;-)
Alt	rs1060499637(-;-)
Reference	Rs1060499637(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.241669399delA
CLNSRC
CLNACC	RCV000445636.1,