rs1060499636

Orientation

minus

Stabilized

minus

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

Make rs1060499636(G;G)

Make rs1060499636(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241508610

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499636
dbSNP (classic)	rs1060499636
ClinGen	rs1060499636
ebi	rs1060499636
HLI	rs1060499636
Exac	rs1060499636
Gnomad	rs1060499636
Varsome	rs1060499636
LitVar	rs1060499636
Map	rs1060499636
PheGenI	rs1060499636
Biobank	rs1060499636
1000 genomes	rs1060499636
hgdp	rs1060499636
ensembl	rs1060499636
geneview	rs1060499636
scholar	rs1060499636
google	rs1060499636
pharmgkb	rs1060499636
gwascentral	rs1060499636
openSNP	rs1060499636
23andMe	rs1060499636
SNPshot	rs1060499636
SNPdbe	rs1060499636
MSV3d	rs1060499636
GWAS Ctlg	rs1060499636

Max Magnitude

0

ClinVar
Risk	rs1060499636(G;G)
Alt	rs1060499636(G;G)
Reference	Rs1060499636(T;T)
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.241671910A>C
CLNSRC
CLNACC	RCV000445612.1,