rs1064795320

Orientation

minus

Stabilized

minus

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

Chromosome

1

Position

241497972

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs1064795320
dbSNP (classic)	rs1064795320
ClinGen	rs1064795320
ebi	rs1064795320
HLI	rs1064795320
Exac	rs1064795320
Gnomad	rs1064795320
Varsome	rs1064795320
LitVar	rs1064795320
Map	rs1064795320
PheGenI	rs1064795320
Biobank	rs1064795320
1000 genomes	rs1064795320
hgdp	rs1064795320
ensembl	rs1064795320
geneview	rs1064795320
scholar	rs1064795320
google	rs1064795320
pharmgkb	rs1064795320
gwascentral	rs1064795320
openSNP	rs1064795320
23andMe	rs1064795320
SNPshot	rs1064795320
SNPdbe	rs1064795320
MSV3d	rs1064795320
GWAS Ctlg	rs1064795320

Max Magnitude

0

ClinVar
Risk	rs1064795320(-;-)
Alt	rs1064795320(-;-)
Reference	Rs1064795320(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241661272delT
CLNSRC
CLNACC	RCV000486287.1,