rs137852447

Orientation

minus

Stabilized

minus

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

Make rs137852447(A;T)

Make rs137852447(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154904861

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852447
dbSNP (classic)	rs137852447
ClinGen	rs137852447
ebi	rs137852447
HLI	rs137852447
Exac	rs137852447
Gnomad	rs137852447
Varsome	rs137852447
LitVar	rs137852447
Map	rs137852447
PheGenI	rs137852447
Biobank	rs137852447
1000 genomes	rs137852447
hgdp	rs137852447
ensembl	rs137852447
geneview	rs137852447
scholar	rs137852447
google	rs137852447
pharmgkb	rs137852447
gwascentral	rs137852447
openSNP	rs137852447
23andMe	rs137852447
SNPshot	rs137852447
SNPdbe	rs137852447
MSV3d	rs137852447
GWAS Ctlg	rs137852447

Max Magnitude

0

OMIM	306700
Desc
Variant	0200
Related	also

ClinVar
Risk	rs137852447(T;T)
Alt	rs137852447(T;T)
Reference	Rs137852447(A;A)
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.154133136T>A
CLNSRC
CLNACC