rs137852410

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;G)	3.5	Carrier of a Hemophilia A mutation
(G;G)	0	common in clinvar

Make rs137852410(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154966654

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852410
dbSNP (classic)	rs137852410
ClinGen	rs137852410
ebi	rs137852410
HLI	rs137852410
Exac	rs137852410
Gnomad	rs137852410
Varsome	rs137852410
LitVar	rs137852410
Map	rs137852410
PheGenI	rs137852410
Biobank	rs137852410
1000 genomes	rs137852410
hgdp	rs137852410
ensembl	rs137852410
geneview	rs137852410
scholar	rs137852410
google	rs137852410
pharmgkb	rs137852410
gwascentral	rs137852410
openSNP	rs137852410
23andMe	rs137852410
SNPshot	rs137852410
SNPdbe	rs137852410
MSV3d	rs137852410
GWAS Ctlg	rs137852410

Max Magnitude

3.5

OMIM	306700
Desc
Variant	0119
Related	also

ClinVar
Risk	rs137852410(C;C)
Alt	rs137852410(C;C)
Reference	Rs137852410(G;G)
Significance	Pathogenic
Disease	Hereditary factor VIII deficiency disease
Variation	info
Gene	F8
CLNDBN	Hereditary factor VIII deficiency disease
Reversed	1
HGVS	NC_000023.10:g.154194929C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010915.6,