rs768182640

Orientation

plus

Stabilized

plus

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

Make rs768182640(-;CA)

Make rs768182640(CA;CA)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

241511968

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs768182640
dbSNP (classic)	rs768182640
ClinGen	rs768182640
ebi	rs768182640
HLI	rs768182640
Exac	rs768182640
Gnomad	rs768182640
Varsome	rs768182640
LitVar	rs768182640
Map	rs768182640
PheGenI	rs768182640
Biobank	rs768182640
1000 genomes	rs768182640
hgdp	rs768182640
ensembl	rs768182640
geneview	rs768182640
scholar	rs768182640
google	rs768182640
pharmgkb	rs768182640
gwascentral	rs768182640
openSNP	rs768182640
23andMe	rs768182640
SNPshot	rs768182640
SNPdbe	rs768182640
MSV3d	rs768182640
GWAS Ctlg	rs768182640

Max Magnitude

0

ClinVar
Risk	rs768182640(CA;CA)
Alt	rs768182640(CA;CA)
Reference	Rs768182640(-;-)
Significance	Pathogenic
Disease	Hereditary leiomyomatosis and renal cell cancer not provided
Variation	info
Gene	FH
CLNDBN	Hereditary leiomyomatosis and renal cell cancer not provided
Reversed	0
HGVS	NC_000001.10:g.241675268_241675269insCA
CLNSRC
CLNACC	RCV000445584.1, RCV000486167.1,