rs1060499629

Orientation

minus

Stabilized

minus

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

Make rs1060499629(-;-)

Make rs1060499629(-;GTAAGTGGCA)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241517172

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1060499629
dbSNP (classic)	rs1060499629
ClinGen	rs1060499629
ebi	rs1060499629
HLI	rs1060499629
Exac	rs1060499629
Gnomad	rs1060499629
Varsome	rs1060499629
LitVar	rs1060499629
Map	rs1060499629
PheGenI	rs1060499629
Biobank	rs1060499629
1000 genomes	rs1060499629
hgdp	rs1060499629
ensembl	rs1060499629
geneview	rs1060499629
scholar	rs1060499629
google	rs1060499629
pharmgkb	rs1060499629
gwascentral	rs1060499629
openSNP	rs1060499629
23andMe	rs1060499629
SNPshot	rs1060499629
SNPdbe	rs1060499629
MSV3d	rs1060499629
GWAS Ctlg	rs1060499629

Max Magnitude

0

ClinVar
Risk	rs1060499629(-;-)
Alt	rs1060499629(-;-)
Reference	Rs1060499629(GTAAGTGGCA;GTAAGTGGCA)
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.241680472_241680481delTGCCACTTAC
CLNSRC
CLNACC	RCV000445611.1,