rs137852438

Orientation

minus

Stabilized

minus

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

Make rs137852438(G;T)

Make rs137852438(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154928890

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852438
dbSNP (classic)	rs137852438
ClinGen	rs137852438
ebi	rs137852438
HLI	rs137852438
Exac	rs137852438
Gnomad	rs137852438
Varsome	rs137852438
LitVar	rs137852438
Map	rs137852438
PheGenI	rs137852438
Biobank	rs137852438
1000 genomes	rs137852438
hgdp	rs137852438
ensembl	rs137852438
geneview	rs137852438
scholar	rs137852438
google	rs137852438
pharmgkb	rs137852438
gwascentral	rs137852438
openSNP	rs137852438
23andMe	rs137852438
SNPshot	rs137852438
SNPdbe	rs137852438
MSV3d	rs137852438
GWAS Ctlg	rs137852438

Max Magnitude

0

OMIM	306700
Desc
Variant	0182
Related	also

ClinVar
Risk	rs137852438(T;T)
Alt	rs137852438(T;T)
Reference	Rs137852438(G;G)
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.154157165C>A
CLNSRC
CLNACC