rs137852411

Orientation

minus

Stabilized

minus

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

Make rs137852411(C;C)

Make rs137852411(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

154961138

Gene

F8

is a	snp
is	mentioned by
dbSNP	rs137852411
dbSNP (classic)	rs137852411
ClinGen	rs137852411
ebi	rs137852411
HLI	rs137852411
Exac	rs137852411
Gnomad	rs137852411
Varsome	rs137852411
LitVar	rs137852411
Map	rs137852411
PheGenI	rs137852411
Biobank	rs137852411
1000 genomes	rs137852411
hgdp	rs137852411
ensembl	rs137852411
geneview	rs137852411
scholar	rs137852411
google	rs137852411
pharmgkb	rs137852411
gwascentral	rs137852411
openSNP	rs137852411
23andMe	rs137852411
SNPshot	rs137852411
SNPdbe	rs137852411
MSV3d	rs137852411
GWAS Ctlg	rs137852411

Merged from

Rs28937274

Max Magnitude

0

OMIM	306700
Desc
Variant	0131
Related	also

ClinVar
Risk	rs137852411(C;C)
Alt	rs137852411(C;C)
Reference	Rs137852411(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.154189413A>G
CLNSRC
CLNACC