rs137852370

Orientation

minus

Stabilized

minus

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

Make rs137852370(C;C)

Make rs137852370(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154966655

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852370
dbSNP (classic)	rs137852370
ClinGen	rs137852370
ebi	rs137852370
HLI	rs137852370
Exac	rs137852370
Gnomad	rs137852370
Varsome	rs137852370
LitVar	rs137852370
Map	rs137852370
PheGenI	rs137852370
Biobank	rs137852370
1000 genomes	rs137852370
hgdp	rs137852370
ensembl	rs137852370
geneview	rs137852370
scholar	rs137852370
google	rs137852370
pharmgkb	rs137852370
gwascentral	rs137852370
openSNP	rs137852370
23andMe	rs137852370
SNPshot	rs137852370
SNPdbe	rs137852370
MSV3d	rs137852370
GWAS Ctlg	rs137852370

Max Magnitude

0

OMIM	306700
Desc
Variant	0058
Related	also

ClinVar
Risk	rs137852370(C;C)
Alt	rs137852370(C;C)
Reference	Rs137852370(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary factor VIII deficiency disease
Variation	info
Gene	F8
CLNDBN	Hereditary factor VIII deficiency disease
Reversed	1
HGVS	NC_000023.10:g.154194930A>G
CLNSRC
CLNACC